Trait
Prolinuria
Level of proline in the urine anove the upper limit of normal.
Summary
- Also called
- Proline high in urine
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test7 genes linked to Prolinuria
Changes in these genes cause rare conditions in which Prolinuria 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 |
|---|---|---|
| SLC36A2solute carrier family 36 member 2 | Always | In 2 conditions |
| SLC6A18solute carrier family 6 member 18 | Always | In 1 condition |
| SLC6A19solute carrier family 6 member 19 | Always | In 1 condition |
| SLC6A20solute carrier family 6 member 20 | Always | In 1 condition |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Very often (80–99%) | In 2 conditions |
| PRODHproline dehydrogenase 1 | Often (30–79%) | In 2 conditions |
| OPLAH5-oxoprolinase, ATP-hydrolysing | 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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