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rdmorin edited this page Jul 4, 2024 · 22 revisions

bibliography: 'morinlab.bib' csl: 'NLM.csl' link-citations: true

ETV6

Overview

ETV6 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. The prevalence of mutations in DLBCL has varied across different studies and may occur in as many as 10% of patients. This gene has some recurrent sites of mutations (hot spots) including multiple mutations predicted to affect splicing of ETV6 pre-mRNA. The mutation pattern in DLBCL mplies the preferential accumulation of inactivating mutations. Coding and non-coding mutations in this gene are associated with the MCD genetic subgroup of DLBCL.

History

%%{init: { 'logLevel': 'debug', 'theme': 'dark' } }%%
timeline
    title Publication timing
2012-03-06 : Lohr : DLBCL
2017-05-01 : Albuquerque : DLBCL
2017-10-10 : Reddy : DLBCL
2018-04-12 : Schmitz : DLBCL
2018-05-01 : Chapuy : DLBCL
2018-10-01 : Arthur : DLBCL
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Relevance tier by entity

Entity Tier Description
DLBCL 1 aSHM target and high-confidence DLBCL gene[@lohrDiscoveryPrioritizationSomatic2012a; @albuquerqueEnhancingKnowledgeDiscovery2017a; @reddyGeneticFunctionalDrivers2017]

Mutation incidence in large patient cohorts (GAMBL reanalysis)

Entity source frequency (%)
DLBCL GAMBL genomes 4.97
DLBCL Schmitz cohort 10.43
DLBCL Reddy cohort 5.81
DLBCL Chapuy cohort 10.26

Mutation pattern and selective pressure estimates

Entity aSHM Significant selection dN/dS (missense) dN/dS (nonsense)
BL Yes No 1.527 0.000
DLBCL Yes Yes 2.366 28.723
FL Yes No 2.772 0.000

aSHM regions

chr_name hg19_start hg19_end region regulatory_comment
chr12 11796001 11812968 TSS strong_enhancer

ETV6 Hotspots

Chromosome Coordinate (hg19) ref>alt HGVSp
chr12 11803078 C>T A6V
chr12 11803087 G>A S9N
chr12 11803094 G>A K11=

View coding variants in ProteinPaint hg19 or hg38

View all variants in GenomePaint hg19 or hg38

ETV6 Expression

References

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