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rdmorin edited this page Jul 4, 2024 · 25 revisions

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

FBXO11

Overview

Somatic mutations in FBXO11 are common in BL[@richterRecurrentMutationID32012a] and appear in a small number of DLBCLs.[@hubschmannMutationalMechanismsShaping2021b] This gene has some recurrent sites of mutations (hot spots). Mutations lead to stabilization of BCL6, an important transcriptional repressor involved in lymphomagenesis. These mutations present a potential novel target for therapeutic intervention, particularly through strategies aimed at degrading BCL6 or inhibiting its function.

%%{init: { 'logLevel': 'debug', 'theme': 'dark' } }%%
timeline
    title Publication timing
      2012-11-11 : Richter : BL
      2013-12-13 : Parry : MZL
      2018-10-01 : Arthur : DLBCL
      2021-05-05 : Hübschmann : DLBCL
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Relevance tier by entity

Entity Tier Description
MZL 2 relevance in MZL not firmly established[@parryWholeExomeSequencing2013]
BL 1 high-confidence BL gene [@richterRecurrentMutationID32012a]
DLBCL 1 high-confidence DLBCL gene[@hubschmannMutationalMechanismsShaping2021b; @arthurGenomewideDiscoverySomatic2018]

Mutation incidence in large patient cohorts (GAMBL reanalysis)

Entity source frequency (%)
BL GAMBL genomes+capture 23.79
BL Thomas cohort 21.60
BL Panea cohort 15.80
DLBCL GAMBL genomes 3.82
DLBCL Schmitz cohort 2.13
DLBCL Reddy cohort 2.10
DLBCL Chapuy cohort 2.56

Mutation pattern and selective pressure estimates

Entity aSHM Significant selection dN/dS (missense) dN/dS (nonsense)
BL No Yes 14.801 114.063
DLBCL No Yes 2.464 39.449
FL No No 8.837 0.000

FBXO11 hot spots

Chromosome Coordinate Mutation HGVSp
chr2 48040426 T>A N725I
chr2 48040427 T>C N725D
chr2 48040427 T>G N725H
chr2 48040427 T>A N725Y
chr2 48040488 TA>GC I704S
chr2 48040489 A>C I704R
chr2 48040495 T>A N702I
chr2 48040495 T>C N702S
chr2 48040496 T>C N702D
chr2 48040496 T>A N702Y
chr2 48040500 T>A E700D
chr2 48040500 T>G E700D
chr2 48040501 T>A E700V
chr2 48040510 C>T G697D
chr2 48040511 C>G G697R

View coding variants in ProteinPaint hg19 or hg38

View all variants in GenomePaint hg19 or hg38

FBXO11 Expression

References

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