Trait
Thromboembolism
The formation of a blood clot inside a blood vessel that subsequently travels through the blood stream from the site where it formed to another location in the body, generally leading to vascular occlusion at the distant site.
Summary
- Also called
- Blood clot in blood vessel, Thromboembolic disease, Thromboembolic events
Reference genomeGRCh38hg38
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Get my Genome Test51 genes linked to Thromboembolism
Changes in these genes cause rare conditions in which Thromboembolism 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 |
|---|---|---|
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Often (30–79%) | In 1 condition |
| UBA1ubiquitin like modifier activating enzyme 1 | Often (30–79%) | In 1 condition |
| ABCC9ATP binding cassette subfamily C member 9 | Sometimes (5–29%) | In 1 condition |
| EPORerythropoietin receptor | Sometimes (5–29%) | In 1 condition |
| F12coagulation factor XII | Sometimes (5–29%) | In 1 condition |
| GATA4GATA binding protein 4 | Sometimes (5–29%) | In 1 condition |
| GATA5GATA binding protein 5 | Sometimes (5–29%) | In 1 condition |
| GATA6GATA binding protein 6 | Sometimes (5–29%) | In 1 condition |
| GJA5gap junction protein alpha 5 | Sometimes (5–29%) | In 1 condition |
| KCNA5potassium voltage-gated channel subfamily A member 5 | Sometimes (5–29%) | In 1 condition |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Sometimes (5–29%) | In 1 condition |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Sometimes (5–29%) | In 1 condition |
| KCNJ3potassium inwardly rectifying channel subfamily J member 3 | Sometimes (5–29%) | In 1 condition |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Sometimes (5–29%) | In 1 condition |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Sometimes (5–29%) | In 1 condition |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Sometimes (5–29%) | In 1 condition |
| MMACHCmetabolism of cobalamin associated C | Sometimes (5–29%) | In 2 conditions |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Sometimes (5–29%) | In 1 condition |
| MYL4myosin light chain 4 | Sometimes (5–29%) | In 1 condition |
| NKX2-5NK2 homeobox 5 | Sometimes (5–29%) | In 1 condition |
| NKX2-6NK2 homeobox 6 | Sometimes (5–29%) | In 1 condition |
| NPPAnatriuretic peptide A | Sometimes (5–29%) | In 2 conditions |
| NUP155nucleoporin 155 | Sometimes (5–29%) | In 1 condition |
| PDE11Aphosphodiesterase 11A | Sometimes (5–29%) | In 1 condition |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Sometimes (5–29%) | In 1 condition |
| PITX2paired like homeodomain 2 | Sometimes (5–29%) | In 1 condition |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Sometimes (5–29%) | In 2 conditions |
| 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 |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Sometimes (5–29%) | In 1 condition |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Sometimes (5–29%) | In 2 conditions |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Sometimes (5–29%) | In 1 condition |
| TLL1tolloid like 1 | Sometimes (5–29%) | In 1 condition |
| TTNtitin | Sometimes (5–29%) | In 1 condition |
| TTRtransthyretin | Sometimes (5–29%) | In 1 condition |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Rarely (1–4%) | In 1 condition |
| FLNCfilamin C | Rarely (1–4%) | In 1 condition |
| KIF20Akinesin family member 20A | Rarely (1–4%) | In 1 condition |
Show 11 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| MT-CYBmitochondrially encoded cytochrome b | Rarely (1–4%) | In 1 condition |
| MYPNmyopalladin | Rarely (1–4%) | In 1 condition |
| TNNI3troponin I3, cardiac type | Rarely (1–4%) | In 1 condition |
| TNNT2troponin T2, cardiac type | Rarely (1–4%) | In 1 condition |
| CBScystathionine beta-synthase | Not recorded | In 1 condition |
| F13A1coagulation factor XIII A chain | Not recorded | In 1 condition |
| F2coagulation factor II, thrombin | Not recorded | In 1 condition |
| HABP2hyaluronan binding protein 2 | Not recorded | In 1 condition |
| JAK2Janus kinase 2 | Not recorded | In 1 condition |
| MTHFRmethylenetetrahydrofolate reductase | Not recorded | In 1 condition |
| PRDX1peroxiredoxin 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.
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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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