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rdmorin edited this page May 28, 2024 · 19 revisions

MYOM2

Overview

The prevalence of MYOM2 mutations in DLBCL varies across studies. The role of these mutations in lymphomagenesis has not been thoroughly explored.

History

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timeline
    title Publication timing
      2011-07-31 : Pasqualucci : DLBCL
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Relevance tier by entity

Entity Tier Description
DLBCL 1 high-confidence DLBCL gene

Mutation incidence in large patient cohorts (GAMBL reanalysis)

Entity source frequency (%)
DLBCL GAMBL genomes 3.25
DLBCL Schmitz cohort 8.09
DLBCL Reddy cohort 3.20
DLBCL Chapuy cohort 4.27

Mutation pattern and selective pressure estimates

Entity aSHM Significant selection dN/dS (missense) dN/dS (nonsense)
BL No No 2.021 0.000
DLBCL No No 0.893 2.648
FL No No 0.649 12.057

Note

First described in DLBCL in 2011 by Pasqualucci L

View coding variants in ProteinPaint hg19 or hg38

View all variants in GenomePaint hg19 or hg38

image

MYOM2 Expression

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References

  1. Pasqualucci L, Trifonov V, Fabbri G, Ma J, Rossi D, Chiarenza A, Wells VA, Grunn A, Messina M, Elliot O, Chan J, Bhagat G, Chadburn A, Gaidano G, Mullighan CG, Rabadan R, Dalla-Favera R. Analysis of the coding genome of diffuse large B-cell lymphoma. Nat Genet. 2011 Jul 31;43(9):830–837. PMCID: PMC3297422

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