Trait
Blood tumor
Clinical name: Hematological neoplasm
Neoplasms located in the blood and blood-forming tissue (the bone marrow and lymphatic tissue).
Summary
- Also called
- Haematological neoplasm
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test20 genes linked to Blood tumor
Changes in these genes cause rare conditions in which Blood tumor 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 |
|---|---|---|
| ASXL1ASXL transcriptional regulator 1 | Very often (80–99%) | In 2 conditions |
| KITKIT proto-oncogene, receptor tyrosine kinase | Very often (80–99%) | In 1 condition |
| SRSF2serine and arginine rich splicing factor 2 | Very often (80–99%) | In 2 conditions |
| TET2tet methylcytosine dioxygenase 2 | Very often (80–99%) | In 3 conditions |
| CBLCbl proto-oncogene | Sometimes (5–29%) | In 1 condition |
| EPCAMepithelial cell adhesion molecule | Sometimes (5–29%) | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Sometimes (5–29%) | In 1 condition |
| MEFVMEFV innate immunity regulator, pyrin | Sometimes (5–29%) | In 1 condition |
| MLH1mutL homolog 1 | Sometimes (5–29%) | In 1 condition |
| MSH2mutS homolog 2 | Sometimes (5–29%) | In 1 condition |
| MSH6mutS homolog 6 | Sometimes (5–29%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 1 condition |
| PMS1PMS1 homolog 1, mismatch repair system component | Sometimes (5–29%) | In 1 condition |
| PMS2PMS1 homolog 2, mismatch repair system component | Sometimes (5–29%) | In 1 condition |
| PTPN6protein tyrosine phosphatase non-receptor type 6 | Sometimes (5–29%) | In 1 condition |
| RUNX1RUNX family transcription factor 1 | Sometimes (5–29%) | In 1 condition |
| TGFBR2transforming growth factor beta receptor 2 | Sometimes (5–29%) | In 1 condition |
| CALRcalreticulin | Rarely (1–4%) | In 1 condition |
| JAK2Janus kinase 2 | Rarely (1–4%) | In 1 condition |
| MPLMPL proto-oncogene, thrombopoietin receptor | 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.
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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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