Trait
Uterine cancer
Clinical name: Uterine neoplasm
A tumor (abnormal growth of tissue) of the uterus.
Summary
- Also called
- Uterine tumor, Uterine tumour
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Uterine cancer, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test17 genes linked to Uterine cancer
Changes in these genes cause rare conditions in which Uterine 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 |
|---|---|---|
| COL4A5collagen type IV alpha 5 chain | Sometimes (5–29%) | In 1 condition |
| COL4A6collagen type IV alpha 6 chain | Sometimes (5–29%) | In 1 condition |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Sometimes (5–29%) | In 1 condition |
| PTENphosphatase and tensin homolog | Sometimes (5–29%) | In 1 condition |
| ATMATM serine/threonine kinase | Rarely (1–4%) | In 1 condition |
| BMPR1Abone morphogenetic protein receptor type 1A | Rarely (1–4%) | In 1 condition |
| BRCA2BRCA2 DNA repair associated | Rarely (1–4%) | In 1 condition |
| CHEK2checkpoint kinase 2 | Rarely (1–4%) | In 1 condition |
| MUTYHmutY DNA glycosylase | Rarely (1–4%) | In 1 condition |
| NAB2NGFI-A binding protein 2 | Rarely (1–4%) | In 1 condition |
| NPATnuclear protein, coactivator of histone transcription | Rarely (1–4%) | In 1 condition |
| POLD1DNA polymerase delta 1, catalytic subunit | Rarely (1–4%) | In 1 condition |
| POLEDNA polymerase epsilon, catalytic subunit | Rarely (1–4%) | In 1 condition |
| RPS20ribosomal protein S20 | Rarely (1–4%) | In 1 condition |
| SEMA4Asemaphorin 4A | Rarely (1–4%) | In 1 condition |
| STAT6signal transducer and activator of transcription 6 | Rarely (1–4%) | In 1 condition |
| STK11serine/threonine kinase 11 | 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.
Narrower traits
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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks