Trait
Ankylosis
A reduction of joint mobility resulting from changes involving the articular surfaces.
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 Test11 genes linked to Ankylosis
Changes in these genes cause rare conditions in which Ankylosis 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 |
|---|---|---|
| ZMPSTE24zinc metallopeptidase STE24 | Always | In 1 condition |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Very often (80–99%) | In 1 condition |
| PERPp53 apoptosis effector related to PMP22 | Very often (80–99%) | In 1 condition |
| TRPV3transient receptor potential cation channel subfamily V member 3 | Very often (80–99%) | In 1 condition |
| ADGRG6adhesion G protein-coupled receptor G6 | Sometimes (5–29%) | In 1 condition |
| ANKHANKH inorganic pyrophosphate transport regulator | Sometimes (5–29%) | In 1 condition |
| TNFRSF11BTNF receptor superfamily member 11b | Sometimes (5–29%) | In 2 conditions |
| ABCC6ATP binding cassette subfamily C member 6 | Not recorded | In 1 condition |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Not recorded | In 1 condition |
| GNAI3G protein subunit alpha i3 | Not recorded | In 1 condition |
| GNASGNAS complex locus | 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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