Welcome to Lymphopedia!
Overview
This is a comprehensive catalogue of genes that have been nominated as recurrently mutated in one of several common or rare B-cell lymphomas. Each gene is categorized based on the level and quality of supporting data in the original study and other comparable datasets. Details for each gene can be found on their respective pages. The novel genes nominated by each study can be found on the study-centric pages.
To get started, select one of the gene lists from the table below
then select the gene page link for any gene in the table or
explore the genes nominated by individual
studies.
Common B-cell lymphomas
| Entity | Tier 1 (high-confidence) | Tier 2 (low-confidence) | Tier 3 (retired) |
|---|---|---|---|
| BL (tsv) | 32 genes | 72 genes | 70 genes |
| DLBCL (tsv) | 125 genes | 210 genes | 387 genes |
| FL (tsv) | 54 genes | 59 genes | 0 genes |
History of lymphoma genes in common entities
Rare B-cell lymphomas
| Entity | Tier 1 (high-confidence) | Tier 2 (low-confidence) | Tier 3 (retired) |
|---|---|---|---|
| PMBL(tsv) | 76 genes | 82 genes | 0 genes |
| MCL (tsv) | 23 genes | 46 genes | 0 genes |
| MZL (tsv) | 42 genes | 74 genes | 0 genes |
* PMBL gene list includes genes attributed to classical Hodgkin lymphoma or marginal grey-zone lymphoma
History of lymphoma genes in rare entities
Regions commonly affected by aSHM
Origins of the individual lymphoma genes
All studies
Studies selected for manual review
| Study | Sequencing Method | Entity | Tier 1 genes contributed | Genes failing QC |
|---|---|---|---|---|
| Love et al. (2012) | Exome | BL | 3 | 48 (84%) |
| Morin et al. (2013) | WGS | DLBCL | 9 | 7 (24%) |
| Reddy et al. (2017) | Exome | DLBCL | 6 | 29 (55%) |
| Panea et al. (2019) | Exome/RNA-seq | BL | 4 | 22 (55%) |
| Chapuy et al. (2018) | Exome | DLBCL | 2 | 7 (41%) |
| Hübschmann et al. (2021) | WGS | DLBCL,FL | 4 | 3 (9%) |
Categorization of genes
Tiers
Tier 2 - Any gene described as significantly or recurrently mutated in one or more types of B-cell lymphoma is initially assigned to Tier 2 for that entity. The study describing the mutation of that gene in a particular entity is considered the originating study.
Tier 1 - Genes can transition to Tier 1 only after additional studies have demonstrated the recurrence of mutations in the same entity.
Additional Designations
aSHM - Denotes genes as affected by aberrant somatic hypermutation (aSHM). Tier 1 and Tier 2 genes can have this designation, respectively abbreviated as 1-a and 2-a. For example, see BCL7A.
Fail - Some studies with large additions to Tier 2 lists have undergone manual review of the primary data. If the majority of mutations in a gene fail QC, the gene will be given the designation 2-F. For example, see MARK1.


