Trait
Urinary urgency
Urge incontinence is the strong, sudden need to urinate.
Summary
- Also called
- Overactive bladder, Urgent micturition
- Body system
- Abnormality of the genitourinary system
Reference genomeGRCh38hg38
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Get my Genome Test64 genes linked to Urinary urgency
Changes in these genes cause rare conditions in which Urinary urgency 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 |
|---|---|---|
| EIF2AK1eukaryotic translation initiation factor 2 alpha kinase 1 | Always | In 1 condition |
| PLP1proteolipid protein 1 | Always | In 1 condition |
| RAB32RAB32, member RAS oncogene family | Always | In 1 condition |
| LRIG2leucine rich repeats and immunoglobulin like domains 2 | Very often (80–99%) | In 1 condition |
| WASHC5WASH complex subunit 5 | Very often (80–99%) | In 2 conditions |
| ATP13A2ATPase cation transporting 13A2 | Often (30–79%) | In 1 condition |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Often (30–79%) | In 2 conditions |
| CPT1Ccarnitine palmitoyltransferase 1C | Often (30–79%) | In 1 condition |
| FXNfrataxin | Often (30–79%) | In 1 condition |
| KIF5Akinesin family member 5A | Often (30–79%) | In 2 conditions |
| LRRC7leucine rich repeat containing 7 | Often (30–79%) | In 1 condition |
| MARS2methionyl-tRNA synthetase 2, mitochondrial | Often (30–79%) | In 2 conditions |
| PI4KAphosphatidylinositol 4-kinase alpha | Often (30–79%) | In 1 condition |
| PNPT1polyribonucleotide nucleotidyltransferase 1 | Often (30–79%) | In 1 condition |
| RTN2reticulon 2 | Often (30–79%) | In 3 conditions |
| SACSsacsin molecular chaperone | Often (30–79%) | In 1 condition |
| SPASTspastin | Often (30–79%) | In 2 conditions |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Often (30–79%) | In 3 conditions |
| UBAP1ubiquitin associated protein 1 | Often (30–79%) | In 2 conditions |
| ABCD1ATP binding cassette subfamily D member 1 | Sometimes (5–29%) | In 1 condition |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Sometimes (5–29%) | In 2 conditions |
| ALMS1ALMS1 centrosome and basal body associated protein | Sometimes (5–29%) | In 1 condition |
| ATL1atlastin GTPase 1 | Sometimes (5–29%) | In 2 conditions |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| ATXN10ataxin 10 | Sometimes (5–29%) | In 2 conditions |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| CMPK2cytidine/uridine monophosphate kinase 2 | Sometimes (5–29%) | In 1 condition |
| GNB2G protein subunit beta 2 | Sometimes (5–29%) | In 1 condition |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Sometimes (5–29%) | In 1 condition |
| HSPD1heat shock protein family D (Hsp60) member 1 | Sometimes (5–29%) | In 2 conditions |
| JAM2junctional adhesion molecule 2 | Sometimes (5–29%) | In 1 condition |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Sometimes (5–29%) | In 1 condition |
| KPNA3karyopherin subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| LMNB1lamin B1 | Sometimes (5–29%) | In 1 condition |
| MED27mediator complex subunit 27 | Sometimes (5–29%) | In 1 condition |
| MYORGmyogenesis regulating glycosidase | Sometimes (5–29%) | In 1 condition |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Sometimes (5–29%) | In 1 condition |
| PDGFBplatelet derived growth factor subunit B | Sometimes (5–29%) | In 1 condition |
| PDGFRBplatelet derived growth factor receptor beta | Sometimes (5–29%) | In 1 condition |
| REEP1receptor accessory protein 1 | Sometimes (5–29%) | In 1 condition |
Show 24 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| RRP12ribosomal RNA processing 12 homolog | Sometimes (5–29%) | In 1 condition |
| SLC20A2solute carrier family 20 member 2 | Sometimes (5–29%) | In 1 condition |
| TPP1tripeptidyl peptidase 1 | Sometimes (5–29%) | In 1 condition |
| TTPAalpha tocopherol transfer protein | Sometimes (5–29%) | In 1 condition |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Sometimes (5–29%) | In 1 condition |
| ADH1Calcohol dehydrogenase 1C (class I), gamma polypeptide | Not recorded | In 1 condition |
| ATXN2ataxin 2 | Not recorded | In 1 condition |
| ATXN3ataxin 3 | Not recorded | In 1 condition |
| ATXN8OSATXN8 opposite strand lncRNA | Not recorded | In 1 condition |
| COQ2coenzyme Q2, polyprenyltransferase | Not recorded | In 1 condition |
| FA2Hfatty acid 2-hydroxylase | Not recorded | In 1 condition |
| GBA1glucosylceramidase beta 1 | Not recorded | In 1 condition |
| MAPTmicrotubule associated protein tau | Not recorded | In 1 condition |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Not recorded | In 1 condition |
| NIPA1NIPA magnesium transporter 1 | Not recorded | In 1 condition |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Not recorded | In 1 condition |
| PINK1PTEN induced kinase 1 | Not recorded | In 1 condition |
| SNCAsynuclein alpha | Not recorded | In 1 condition |
| SNCAIPsynuclein alpha interacting protein | Not recorded | In 1 condition |
| SPARTspartin | Not recorded | In 1 condition |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Not recorded | In 1 condition |
| TBPTATA-box binding protein | Not recorded | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Not recorded | In 1 condition |
| ZFYVE26zinc finger FYVE-type containing 26 | 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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