Overview
BTG2 is one of a number of genes affected by aberrant somatic hypermutation in B-cell lymphomas, which complicates the interpretation of mutations at this locus. Mutations in the BTG2 gene have been implicated in the pathogenesis of diffuse large B-cell lymphoma (DLBCL), contributing to the development and progression of the disease. These mutations are a feature of the MCD genetic subgroup of DLBCL. The biological function of BTG2 mutations and their role in lymphomagenesis remains poorly understood. Due to minimal support in the original primary data and very few mutations reported in subsequent studies, this gene is very unlikely to be relevant in BL.
Relevance tier by entity
| Entity | Tier | Description |
|---|---|---|
| 3 | Retired, Failed QC1 | |
| 1 | aSHM target and high-confidence DLBCL gene2 | |
| 1 | aSHM target and high-confidence FL gene2 |
Mutation incidence in large patient cohorts (GAMBL reanalysis)
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Cannot include /FL_BTG2.md - does not exist yet
Mutation pattern and selective pressure estimates
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aSHM regions
| chr_name | hg19_start | hg19_end | region | regulatory_comment |
|---|---|---|---|---|
| chr1 | 203274698 | 203275778 | intron | active_promoter |
View coding variants in ProteinPaint hg19 or hg38
View all variants in GenomePaint hg19 or hg38
BTG2 Expression
Representative Mutations
BL1
Rating ★ ★ ☆ ☆
☆
All Mutations
BL1
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