Trait
Multiple joint dislocation
Dislocation of many joints.
Summary
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test12 genes linked to Multiple joint dislocation
Changes in these genes cause rare conditions in which Multiple joint dislocation 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 |
|---|---|---|
| GNB2G protein subunit beta 2 | Always | In 1 condition |
| THBS2thrombospondin 2 | Always | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Very often (80–99%) | In 1 condition |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Very often (80–99%) | In 1 condition |
| CHST3carbohydrate sulfotransferase 3 | Very often (80–99%) | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Very often (80–99%) | In 1 condition |
| COL1A2collagen type I alpha 2 chain | Very often (80–99%) | In 1 condition |
| GZF1GDNF inducible zinc finger protein 1 | Often (30–79%) | In 1 condition |
| KIF22kinesin family member 22 | Often (30–79%) | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Often (30–79%) | In 1 condition |
| TNXBtenascin XB | Often (30–79%) | In 1 condition |
| EXOC6Bexocyst complex component 6B | 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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