Trait
Mini stroke
Clinical name: Transient ischemic attack
Summary
- Also called
- TIA, Transient ischaemic attack, Transient ischaemic attacks, Transient ischemic attacks
Reference genomeGRCh38hg38
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Get my Genome Test64 genes linked to Mini stroke
Changes in these genes cause rare conditions in which Mini stroke 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 |
|---|---|---|
| HTRA1HtrA serine peptidase 1 | Always | In 2 conditions |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Always | In 2 conditions |
| TRIM63tripartite motif containing 63 | Always | In 1 condition |
| GLAgalactosidase alpha | Very often (80–99%) | In 2 conditions |
| ADA2adenosine deaminase 2 | Often (30–79%) | In 1 condition |
| ANGPTL6angiopoietin like 6 | Often (30–79%) | In 1 condition |
| COL3A1collagen type III alpha 1 chain | Often (30–79%) | In 1 condition |
| ENGendoglin | Often (30–79%) | In 3 conditions |
| JAK2Janus kinase 2 | Often (30–79%) | In 2 conditions |
| MPLMPL proto-oncogene, thrombopoietin receptor | Often (30–79%) | In 2 conditions |
| NOS3nitric oxide synthase 3 | Often (30–79%) | In 1 condition |
| NOTCH3notch receptor 3 | Often (30–79%) | In 2 conditions |
| TGFBR3transforming growth factor beta receptor 3 | Often (30–79%) | In 1 condition |
| THPOthrombopoietin | Often (30–79%) | In 1 condition |
| THSD1thrombospondin type 1 domain containing 1 | Often (30–79%) | In 1 condition |
| ABCC6ATP binding cassette subfamily C member 6 | Sometimes (5–29%) | In 2 conditions |
| ACTA2actin alpha 2, smooth muscle | Sometimes (5–29%) | In 1 condition |
| ACTBactin beta | Sometimes (5–29%) | In 1 condition |
| ACTG1actin gamma 1 | Sometimes (5–29%) | In 1 condition |
| ACVRL1activin A receptor like type 1 | Sometimes (5–29%) | In 2 conditions |
| ADAMTS13ADAM metallopeptidase with thrombospondin type 1 motif 13 | Sometimes (5–29%) | In 1 condition |
| CALRcalreticulin | Sometimes (5–29%) | In 1 condition |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Sometimes (5–29%) | In 1 condition |
| ELNelastin | Sometimes (5–29%) | In 1 condition |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Sometimes (5–29%) | In 2 conditions |
| FBN1fibrillin 1 | Sometimes (5–29%) | In 1 condition |
| FOXE3forkhead box E3 | Sometimes (5–29%) | In 1 condition |
| GDF2growth differentiation factor 2 | Sometimes (5–29%) | In 1 condition |
| HEY2hes related family bHLH transcription factor with YRPW motif 2 | Sometimes (5–29%) | In 1 condition |
| HLA-Bmajor histocompatibility complex, class I, B | Sometimes (5–29%) | In 1 condition |
| IL12Binterleukin 12B | Sometimes (5–29%) | In 1 condition |
| LMNAlamin A/C | Sometimes (5–29%) | In 1 condition |
| LOXlysyl oxidase | Sometimes (5–29%) | In 1 condition |
| MAT2Amethionine adenosyltransferase 2A | Sometimes (5–29%) | In 1 condition |
| MFAP5microfibril associated protein 5 | Sometimes (5–29%) | In 1 condition |
| MLXMAX dimerization protein MLX | Sometimes (5–29%) | In 1 condition |
| MYH11myosin heavy chain 11 | Sometimes (5–29%) | In 1 condition |
| MYLKmyosin light chain kinase | Sometimes (5–29%) | In 1 condition |
| PRKG1protein kinase cGMP-dependent 1 | Sometimes (5–29%) | In 1 condition |
| SH2B3SH2B adaptor protein 3 | Sometimes (5–29%) | In 1 condition |
Show 24 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| SMAD2SMAD family member 2 | Sometimes (5–29%) | In 1 condition |
| SMAD3SMAD family member 3 | Sometimes (5–29%) | In 1 condition |
| SMAD4SMAD family member 4 | Sometimes (5–29%) | In 2 conditions |
| SONSON DNA and RNA binding protein | Sometimes (5–29%) | In 1 condition |
| TET2tet methylcytosine dioxygenase 2 | Sometimes (5–29%) | In 1 condition |
| TGFB2transforming growth factor beta 2 | Sometimes (5–29%) | In 1 condition |
| TGFB3transforming growth factor beta 3 | Sometimes (5–29%) | In 1 condition |
| TGFBR1transforming growth factor beta receptor 1 | Sometimes (5–29%) | In 1 condition |
| TGFBR2transforming growth factor beta receptor 2 | Sometimes (5–29%) | In 1 condition |
| THSD4thrombospondin type 1 domain containing 4 | Sometimes (5–29%) | In 1 condition |
| TP53tumor protein p53 | Sometimes (5–29%) | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | Sometimes (5–29%) | In 1 condition |
| ACTC1actin alpha cardiac muscle 1 | Rarely (1–4%) | In 1 condition |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Rarely (1–4%) | In 1 condition |
| GATA4GATA binding protein 4 | Rarely (1–4%) | In 1 condition |
| GATA6GATA binding protein 6 | Rarely (1–4%) | In 1 condition |
| MYH6myosin heavy chain 6 | Rarely (1–4%) | In 1 condition |
| NKX2-5NK2 homeobox 5 | Rarely (1–4%) | In 1 condition |
| TBX20T-box transcription factor 20 | Rarely (1–4%) | In 1 condition |
| TLL1tolloid like 1 | Rarely (1–4%) | In 1 condition |
| ANO1anoctamin 1 | Not recorded | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Not recorded | In 1 condition |
| MYBPC3myosin binding protein C3 | Not recorded | In 1 condition |
| RNF213ring finger protein 213 | 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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