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Trait
Prostate cancer
A cancer of the prostate.
Summary
- Also called
- Prostatic cancer
Prostate cancerHP:0012125
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Get my Genome Test33 genes linked to Prostate cancer
Changes in these genes cause rare conditions in which Prostate cancer 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 |
|---|---|---|
| RNASELribonuclease L | Always | In 1 condition |
| ATMATM serine/threonine kinase | Sometimes (5–29%) | In 1 condition |
| BARD1BRCA1 associated RING domain 1 | Sometimes (5–29%) | In 1 condition |
| BRCA1BRCA1 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| BRCA2BRCA2 DNA repair associated | Sometimes (5–29%) | In 2 conditions |
| BRIP1BRCA1 interacting DNA helicase 1 | Sometimes (5–29%) | In 1 condition |
| CHEK2checkpoint kinase 2 | Sometimes (5–29%) | In 3 conditions |
| FOXE1forkhead box E1 | Sometimes (5–29%) | In 1 condition |
| MRE11MRE11 double strand break repair nuclease | Sometimes (5–29%) | In 1 condition |
| NBNnibrin | Sometimes (5–29%) | In 1 condition |
| NTHL1nth like DNA glycosylase 1 | Sometimes (5–29%) | In 1 condition |
| PALB2partner and localizer of BRCA2 | Sometimes (5–29%) | In 1 condition |
| PTENphosphatase and tensin homolog | Sometimes (5–29%) | In 2 conditions |
| RAD50RAD50 double strand break repair protein | Sometimes (5–29%) | In 1 condition |
| RAD51RAD51 recombinase | Sometimes (5–29%) | In 1 condition |
| RAD51CRAD51 paralog C | Sometimes (5–29%) | In 1 condition |
| RAD51DRAD51 paralog D | Sometimes (5–29%) | In 1 condition |
| TP53tumor protein p53 | Sometimes (5–29%) | In 3 conditions |
| AAGABalpha and gamma adaptin binding protein | Rarely (1–4%) | In 1 condition |
| BMPR1Abone morphogenetic protein receptor type 1A | Rarely (1–4%) | In 1 condition |
| CDKN2Acyclin dependent kinase inhibitor 2A | Rarely (1–4%) | In 1 condition |
| COL14A1collagen type XIV alpha 1 chain | Rarely (1–4%) | In 1 condition |
| GREM1gremlin 1, DAN family BMP antagonist | Rarely (1–4%) | In 1 condition |
| MDM2MDM2 proto-oncogene | Rarely (1–4%) | In 1 condition |
| NAB2NGFI-A binding protein 2 | Rarely (1–4%) | In 1 condition |
| RNF43ring finger protein 43 | Rarely (1–4%) | In 1 condition |
| STAT6signal transducer and activator of transcription 6 | Rarely (1–4%) | In 1 condition |
| ARandrogen receptor | Not recorded | In 1 condition |
| EPHB2EPH receptor B2 | Not recorded | In 1 condition |
| KLF6KLF transcription factor 6 | Not recorded | In 1 condition |
| MAD1L1mitotic arrest deficient 1 like 1 | Not recorded | In 1 condition |
| MXI1MAX interactor 1, dimerization protein | Not recorded | In 1 condition |
| ZFHX3zinc finger homeobox 3 | 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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