Trait
Overtubulated long bones
Overconstriction, or narrowness of the diaphysis and metaphysis of long bones.
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 Test6 genes linked to Overtubulated long bones
Changes in these genes cause rare conditions in which Overtubulated long bones 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 |
|---|---|---|
| COG4component of oligomeric golgi complex 4 | Always | In 1 condition |
| LMNAlamin A/C | Often (30–79%) | In 1 condition |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Rarely (1–4%) | In 1 condition |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Rarely (1–4%) | In 1 condition |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Rarely (1–4%) | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | 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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