Trait
Brain neoplasm
A benign or malignant neoplasm that arises from or metastasizes to the brain.
Summary
- Also called
- Brain tumor, Brain tumour
Reference genomeGRCh38hg38
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Get my Genome Test14 genes linked to Brain neoplasm
Changes in these genes cause rare conditions in which Brain neoplasm 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 |
|---|---|---|
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Sometimes (5–29%) | In 1 condition |
| NF1neurofibromin 1 | Sometimes (5–29%) | In 1 condition |
| POLD1DNA polymerase delta 1, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| POLEDNA polymerase epsilon, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| AAGABalpha and gamma adaptin binding protein | Rarely (1–4%) | In 1 condition |
| APCAPC regulator of Wnt signaling pathway | Rarely (1–4%) | In 1 condition |
| COL14A1collagen type XIV alpha 1 chain | Rarely (1–4%) | In 1 condition |
| CHMP2Bcharged multivesicular body protein 2B | Not recorded | In 1 condition |
| GRNgranulin precursor | Not recorded | In 1 condition |
| MAPTmicrotubule associated protein tau | Not recorded | In 1 condition |
| PSEN1presenilin 1 | Not recorded | In 1 condition |
| TMEM106Btransmembrane protein 106B | Not recorded | In 1 condition |
| TREM2triggering receptor expressed on myeloid cells 2 | Not recorded | In 1 condition |
| VCPvalosin containing protein | 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.
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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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