Trait
Knee dislocation
Summary
- Also called
- Dislocations of the knees, Knee dislocations
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test14 genes linked to Knee dislocation
Changes in these genes cause rare conditions in which Knee 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 |
|---|---|---|
| AEBP1AE binding protein 1 | Always | In 2 conditions |
| CHST3carbohydrate sulfotransferase 3 | Always | In 2 conditions |
| DONSONDNA replication fork stabilization factor DONSON | Always | In 1 condition |
| EXOC6Bexocyst complex component 6B | Always | In 1 condition |
| FLNBfilamin B | Always | In 4 conditions |
| HNRNPH1heterogeneous nuclear ribonucleoprotein H1 | Always | In 1 condition |
| IFT56intraflagellar transport 56 | Always | In 1 condition |
| SLC35A3solute carrier family 35 member A3 | Always | In 2 conditions |
| XYLT1xylosyltransferase 1 | Very often (80–99%) | In 1 condition |
| BPNT23'(2'), 5'-bisphosphate nucleotidase 2 | Often (30–79%) | In 1 condition |
| SLC35B2solute carrier family 35 member B2 | Often (30–79%) | In 1 condition |
| RYR1ryanodine receptor 1 | Sometimes (5–29%) | In 1 condition |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Not recorded | In 1 condition |
| SLC10A7solute carrier family 10 member 7 | 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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