NSD2

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

Across TCGA patient cohorts, NSD2 mutation is significantly associated with the total protein of many other genes, with 74 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NSD2-associated genes across cancer lineages are PCNA, STAT3_pY705, and FoxM1. Each is linked with NSD2 in more than 3 cancer types. Because this analysis shows association rather than direction, both NSD2-to-partner and partner-to-NSD2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PCNA grouped by NSD2-low versus NSD2-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NSD2→partner) and Y-score (partner→NSD2) 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
COADPCNA →+0.402+3.000<.001.03434
UCECSTAT3_pY705 →-0.387-2.201<.001<.00134
STADFoxM1 →+0.302+2.201.006.03133
UCECCyclin-B1 →+0.685+2.146<.001<.00133
UCECeEF2 →+0.375+3.169<.001<.00133
UCECACVRL1 →-0.110-1.664.005.01933
Each partner links to its Q-omics profile. Showing the 6 strongest of 74 associations by consensus.

PCNA by NSD2 expression — COAD

Box plot of PCNA in NSD2-low vs NSD2-high samples in COAD.

Explore this box plot interactively →

Exploration