MSH2

mutation — cross-omics
Cross-omicsMUTATION → RNAPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, MSH2 mutation is significantly associated with the RNA expression of many other genes, with 2,397 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MSH2-associated genes across cancer lineages are GTF2A2, NCAPD3, and PKN3. Each is linked with MSH2 in more than 2 cancer types. Because this analysis shows association rather than direction, both MSH2-to-partner and partner-to-MSH2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, GTF2A2 grouped by MSH2-low versus MSH2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (MSH2→partner) and Y-score (partner→MSH2) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
UCECGTF2A2 →+0.378+2.024.003.00133
UCECNCAPD3 →+0.493+2.078.001<.00133
UCECPKN3 →+0.683+2.180<.001<.00133
UCECZNF367 →+0.606+1.928<.001.00833
UCECNIPA1 →+0.683+2.392<.001<.00133
READOR12D1 →+0.108+6.257<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,397 associations by consensus.

GTF2A2 by MSH2 expression — UCEC

Box plot of GTF2A2 in MSH2-low vs MSH2-high samples in UCEC.

Explore this box plot interactively →

Exploration