Trait
Ventricular arrhythmia
Summary
- Also called
- Ventricular arrhythmias
- Body system
- Abnormality of the cardiovascular system
Reference genomeGRCh38hg38
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Get my Genome Test45 genes linked to Ventricular arrhythmia
Changes in these genes cause rare conditions in which Ventricular arrhythmia 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 |
|---|---|---|
| ACTBactin beta | Always | In 1 condition |
| DSG2desmoglein 2 | Always | In 1 condition |
| JUPjunction plakoglobin | Always | In 2 conditions |
| LMNAlamin A/C | Always | In 4 conditions |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Always | In 1 condition |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Often (30–79%) | In 2 conditions |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Often (30–79%) | In 1 condition |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Often (30–79%) | In 1 condition |
| ACTC1actin alpha cardiac muscle 1 | Sometimes (5–29%) | In 1 condition |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Sometimes (5–29%) | In 2 conditions |
| CDH23cadherin related 23 | Sometimes (5–29%) | In 1 condition |
| KCNH2potassium voltage-gated channel subfamily H member 2 | Sometimes (5–29%) | In 1 condition |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Sometimes (5–29%) | In 1 condition |
| LDB3LIM domain binding 3 | Sometimes (5–29%) | In 1 condition |
| POLGDNA polymerase gamma, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| POLG2DNA polymerase gamma 2, accessory subunit | Sometimes (5–29%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sometimes (5–29%) | In 1 condition |
| SLC25A4solute carrier family 25 member 4 | Sometimes (5–29%) | In 1 condition |
| SLC4A3solute carrier family 4 member 3 | Sometimes (5–29%) | In 1 condition |
| TWNKtwinkle mtDNA helicase | Sometimes (5–29%) | In 1 condition |
| ABCC9ATP binding cassette subfamily C member 9 | Rarely (1–4%) | In 1 condition |
| AKAP9A-kinase anchoring protein 9 | Rarely (1–4%) | In 1 condition |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Rarely (1–4%) | In 2 conditions |
| CACNB2calcium voltage-gated channel auxiliary subunit beta 2 | Rarely (1–4%) | In 1 condition |
| GPD1Lglycerol-3-phosphate dehydrogenase 1 like | Rarely (1–4%) | In 1 condition |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Rarely (1–4%) | In 1 condition |
| KCND3potassium voltage-gated channel subfamily D member 3 | Rarely (1–4%) | In 1 condition |
| KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3 | Rarely (1–4%) | In 1 condition |
| KCNE5potassium voltage-gated channel subfamily E regulatory subunit 5 | Rarely (1–4%) | In 1 condition |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Rarely (1–4%) | In 1 condition |
| PKP2plakophilin 2 | Rarely (1–4%) | In 1 condition |
| RANGRFRAN guanine nucleotide release factor | Rarely (1–4%) | In 1 condition |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Rarely (1–4%) | In 1 condition |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Rarely (1–4%) | In 1 condition |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Rarely (1–4%) | In 1 condition |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Rarely (1–4%) | In 1 condition |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Rarely (1–4%) | In 1 condition |
| SCNN1Asodium channel epithelial 1 subunit alpha | Rarely (1–4%) | In 1 condition |
| SEMA3Asemaphorin 3A | Rarely (1–4%) | In 1 condition |
| SLMAPsarcolemma associated protein | Rarely (1–4%) | In 1 condition |
Show 5 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TRPM4transient receptor potential cation channel subfamily M member 4 | Rarely (1–4%) | In 1 condition |
| CAV3caveolin 3 | Not recorded | In 1 condition |
| DSC2desmocollin 2 | Not recorded | In 1 condition |
| DTNAdystrobrevin alpha | Not recorded | In 1 condition |
| PLNphospholamban | 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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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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