Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Spastic/hyperactive bladder, and the rest of your genome, with one test.
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Get my Genome Test11 genes linked to Spastic/hyperactive bladder
Changes in these genes cause rare conditions in which Spastic/hyperactive bladder 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 |
|---|---|---|
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Often (30–79%) | In 1 condition |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Often (30–79%) | In 1 condition |
| GBA1glucosylceramidase beta 1 | Often (30–79%) | In 1 condition |
| GIGYF2GRB10 interacting GYF protein 2 | Often (30–79%) | In 1 condition |
| KIF5Akinesin family member 5A | Often (30–79%) | In 1 condition |
| LRRK2leucine rich repeat kinase 2 | Often (30–79%) | In 1 condition |
| PLP1proteolipid protein 1 | Often (30–79%) | In 1 condition |
| SNCAsynuclein alpha | Often (30–79%) | In 1 condition |
| VPS35VPS35 retromer complex component | Often (30–79%) | In 1 condition |
| LRIG2leucine rich repeats and immunoglobulin like domains 2 | Sometimes (5–29%) | In 1 condition |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Rarely (1–4%) | 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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