SENP2

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

Across TCGA patient cohorts, SENP2 mutation is significantly associated with the RNA expression of many other genes, with 2,104 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SENP2-associated genes across cancer lineages are RN7SKP260, MIR3978, and C14orf177. Each is linked with SENP2 in more than 3 cancer types. Because this analysis shows association rather than direction, both SENP2-to-partner and partner-to-SENP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SKP260 grouped by SENP2-low versus SENP2-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SENP2→partner) and Y-score (partner→SENP2) 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
HNSCRN7SKP260 →+1.526+5.124<.001.00834
HNSCMIR3978 →+1.127+5.655<.001.00434
BRCAC14orf177 →+0.043+4.610<.001.00833
HNSCPSMA5P1 →+0.260+6.763<.001<.00133
HNSCNDUFA5P5 →+0.567+5.435<.001.00533
HNSCOR4N1P →+0.092+5.368<.001.00533
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,104 associations by consensus.

RN7SKP260 by SENP2 expression — HNSC

Box plot of RN7SKP260 in SENP2-low vs SENP2-high samples in HNSC.

Explore this box plot interactively →

Exploration