Trait
Torsade de pointes
A type of ventricular tachycardia characterized by polymorphioc QRS complexes that change in amplitue and cycle length, and thus have the appearance of oscillating around the baseline in the EKG.
Summary
- Also called
- Torsades de pointes
- Body system
- Abnormality of the cardiovascular system
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
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page$trait$nameRead the genes linked to Torsade de pointes, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Torsade de pointes
Changes in these genes cause rare conditions in which Torsade de pointes 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 |
|---|---|---|
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Always | In 1 condition |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Always | In 1 condition |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Often (30–79%) | In 3 conditions |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Often (30–79%) | In 1 condition |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Often (30–79%) | In 3 conditions |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Sometimes (5–29%) | In 1 condition |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Sometimes (5–29%) | In 2 conditions |
| TANGO2transport and golgi organization 2 homolog | Sometimes (5–29%) | In 1 condition |
| RYR2ryanodine receptor 2 | Rarely (1–4%) | In 1 condition |
| ALG10BALG10 alpha-1,2-glucosyltransferase B | Not recorded | In 1 condition |
| KCNH2potassium voltage-gated channel subfamily H member 2 | Not recorded | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Not recorded | In 1 condition |
| SNTA1syntrophin alpha 1 | 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.
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 2026.10.16-c6eea6bf.
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