Trait
Ovotestis
A gonad that contains both ovarian follicles and testicular tubular elements.
Summary
- Body system
- Abnormality of the genitourinary system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test8 genes linked to Ovotestis
Changes in these genes cause rare conditions in which Ovotestis 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 |
|---|---|---|
| SOX9SRY-box transcription factor 9 | Very often (80–99%) | In 2 conditions |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Often (30–79%) | In 1 condition |
| WNT4Wnt family member 4 | Often (30–79%) | In 1 condition |
| SRYsex determining region Y | Sometimes (5–29%) | In 2 conditions |
| COX7Bcytochrome c oxidase subunit 7B | Not recorded | In 1 condition |
| HCCSholocytochrome c synthase | Not recorded | In 1 condition |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Not recorded | In 1 condition |
| RSPO1R-spondin 1 | 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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