Trait
Dysgyria
An abnormal gyral pattern characterized by abnormalities of sulcal depth or orientation.
Summary
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Dysgyria, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test9 genes linked to Dysgyria
Changes in these genes cause rare conditions in which Dysgyria 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 |
|---|---|---|
| SPOUT1SPOUT domain containing methyltransferase 1 | Always | In 1 condition |
| ACTA2actin alpha 2, smooth muscle | Very often (80–99%) | In 1 condition |
| TUBA1Atubulin alpha 1a | Very often (80–99%) | In 1 condition |
| TUBB2Btubulin beta 2B class IIb | Very often (80–99%) | In 1 condition |
| TUBB3tubulin beta 3 class III | Very often (80–99%) | In 1 condition |
| LAMB1laminin subunit beta 1 | Often (30–79%) | In 1 condition |
| MED11mediator complex subunit 11 | Often (30–79%) | In 1 condition |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Often (30–79%) | In 1 condition |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Often (30–79%) | 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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks