Trait
Ventricular tachycardia
A tachycardia originating in the ventricles characterized by rapid heart rate (over 100 beats per minute) and broad QRS complexes (over 120 ms).
Summary
- Body system
- Abnormality of the cardiovascular system
Reference genomeGRCh38hg38
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Get my Genome Test51 genes linked to Ventricular tachycardia
Changes in these genes cause rare conditions in which Ventricular 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 |
|---|---|---|
| ABCC9ATP binding cassette subfamily C member 9 | Always | In 1 condition |
| CPT2carnitine palmitoyltransferase 2 | Always | In 1 condition |
| CRYABcrystallin alpha B | Always | In 1 condition |
| DSPdesmoplakin | Always | In 3 conditions |
| EMDemerin | Always | In 1 condition |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Always | In 1 condition |
| MYH6myosin heavy chain 6 | Always | In 1 condition |
| NRAPnebulin related anchoring protein | Always | In 1 condition |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Always | In 2 conditions |
| TBX5T-box transcription factor 5 | Always | In 1 condition |
| TECRLtrans-2,3-enoyl-CoA reductase like | Always | In 1 condition |
| TGFB3transforming growth factor beta 3 | Always | In 1 condition |
| PKP2plakophilin 2 | Very often (80–99%) | In 1 condition |
| SLC25A20solute carrier family 25 member 20 | Very often (80–99%) | In 2 conditions |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Often (30–79%) | In 1 condition |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Often (30–79%) | In 1 condition |
| CTNNA3catenin alpha 3 | Often (30–79%) | In 1 condition |
| DSG2desmoglein 2 | Often (30–79%) | In 1 condition |
| GYG1glycogenin 1 | Often (30–79%) | In 1 condition |
| LAMP2lysosome associated membrane protein 2 | Often (30–79%) | In 1 condition |
| MT-CYBmitochondrially encoded cytochrome b | Often (30–79%) | In 1 condition |
| MYZAPmyocardial zonula adherens protein | Often (30–79%) | In 1 condition |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Often (30–79%) | In 1 condition |
| POPDC2popeye domain cAMP effector 2 | Often (30–79%) | In 1 condition |
| RYR1ryanodine receptor 1 | Often (30–79%) | In 1 condition |
| TANGO2transport and golgi organization 2 homolog | Often (30–79%) | In 1 condition |
| ACTC1actin alpha cardiac muscle 1 | Sometimes (5–29%) | In 1 condition |
| BTNL2butyrophilin like 2 | Sometimes (5–29%) | In 1 condition |
| CALM1calmodulin 1 | Sometimes (5–29%) | In 1 condition |
| CDH2cadherin 2 | Sometimes (5–29%) | In 1 condition |
| CRELD1CRELD disulfide isomerase 1 | Sometimes (5–29%) | In 1 condition |
| CSRP3cysteine and glycine rich protein 3 | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 1 condition |
| JPH2junctophilin 2 | Sometimes (5–29%) | In 1 condition |
| LMNAlamin A/C | Sometimes (5–29%) | In 1 condition |
| MYH7myosin heavy chain 7 | Sometimes (5–29%) | In 1 condition |
| MYOZ2myozenin 2 | Sometimes (5–29%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Sometimes (5–29%) | In 1 condition |
| NPPAnatriuretic peptide A | Sometimes (5–29%) | In 1 condition |
| PPP1R13Lprotein phosphatase 1 regulatory subunit 13 like | Sometimes (5–29%) | In 1 condition |
Show 11 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TPM1tropomyosin 1 | Sometimes (5–29%) | In 1 condition |
| ACADVLacyl-CoA dehydrogenase very long chain | Rarely (1–4%) | In 1 condition |
| SLC12A3solute carrier family 12 member 3 | Rarely (1–4%) | In 1 condition |
| BAG5BAG cochaperone 5 | Not recorded | In 1 condition |
| CASQ2calsequestrin 2 | Not recorded | In 2 conditions |
| JUPjunction plakoglobin | Not recorded | In 1 condition |
| MYL2myosin light chain 2 | Not recorded | In 1 condition |
| RYR2ryanodine receptor 2 | Not recorded | In 1 condition |
| TMEM43transmembrane protein 43 | Not recorded | In 1 condition |
| TRDNtriadin | Not recorded | In 1 condition |
| TTNtitin | 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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