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Traits
Traits linked to KCNE1
potassium voltage-gated channel subfamily E regulatory subunit 1
The Human Phenotype Ontology links 26 traits to KCNE1, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Extra heart beat | Always |
| Fainting spell | Always |
| Prolonged QT interval | Always |
| Sinus bradycardia | Always |
| Prolonged QTc interval | Very often (80–99%) |
| Abnormal heart rate | Often (30–79%) |
| Palpitations | Often (30–79%) |
| Quivering upper heart chambers resulting in irregular heartbeat | Often (30–79%) |
| Torsade de pointes | Often (30–79%) |
| Ventricular fibrillation | Often (30–79%) |
| Heart attack | Sometimes (5–29%) |
| Sudden cardiac death | Not recorded |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Congenital sensorineural hearing impairment | Always |
| Bilateral sensorineural hearing impairment | Very often (80–99%) |
| Profound sensorineural hearing impairment | Very often (80–99%) |
| Dizziness | Often (30–79%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Chest pain | Often (30–79%) |
| Decreased ability to exercise | Often (30–79%) |
| Fatigue | Often (30–79%) |
| Postexertional symptom exacerbation | Often (30–79%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Iron deficiency anemia | Sometimes (5–29%) |
| Thromboembolic stroke | Sometimes (5–29%) |
| Thromboembolism | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Loss of consciousness | Often (30–79%) |
| Epilepsy | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Breathing difficulty | Often (30–79%) |
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.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to KCNE1 and how often each is seen. Find out more at hpo.jax.org.
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