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Trait
B-cell lymphoma
A type of lymphoma that originates in B-cells.
Summary
- Also called
- B cell lymphoma
B-cell lymphomaHP:0012191
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Read the genes linked to B-cell lymphoma, and the rest of your genome, with one test.
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Get my Genome Test24 genes linked to B-cell lymphoma
Changes in these genes cause rare conditions in which B-cell lymphoma 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 |
|---|---|---|
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| MAGT1magnesium transporter 1 | Always | In 1 condition |
| NFATC2nuclear factor of activated T cells 2 | Always | In 1 condition |
| PTPRCprotein tyrosine phosphatase receptor type C | Always | In 1 condition |
| RASGRP1RAS guanyl releasing protein 1 | Always | In 1 condition |
| ATMATM serine/threonine kinase | Very often (80–99%) | In 1 condition |
| BCL10BCL10 immune signaling adaptor | Very often (80–99%) | In 1 condition |
| BIRC3baculoviral IAP repeat containing 3 | Very often (80–99%) | In 1 condition |
| CCND1cyclin D1 | Very often (80–99%) | In 1 condition |
| FOXP1forkhead box P1 | Very often (80–99%) | In 1 condition |
| IGHimmunoglobulin heavy locus | Very often (80–99%) | In 2 conditions |
| MALT1MALT1 paracaspase | Very often (80–99%) | In 1 condition |
| IKZF3IKAROS family zinc finger 3 | Often (30–79%) | In 1 condition |
| ITKIL2 inducible T cell kinase | Often (30–79%) | In 1 condition |
| SYKspleen associated tyrosine kinase | Often (30–79%) | In 1 condition |
| CASP10caspase 10 | Sometimes (5–29%) | In 1 condition |
| DIAPH1diaphanous related formin 1 | Sometimes (5–29%) | In 1 condition |
| FASFas cell surface death receptor | Sometimes (5–29%) | In 1 condition |
| FASLGFas ligand | Sometimes (5–29%) | In 1 condition |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | Sometimes (5–29%) | In 1 condition |
| NBNnibrin | Sometimes (5–29%) | In 1 condition |
| STAT6signal transducer and activator of transcription 6 | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Rarely (1–4%) | In 1 condition |
| ADAadenosine deaminase | 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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