SENP2

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

Across TCGA cell cohorts, SENP2 mutation is significantly associated with the RNA expression of many other genes, with 3 significant associations in total. CNS shows the largest number of these associations.

The most reproducible SENP2-associated genes across cancer lineages are CCER1, PRAMEF7, and PRAMEF5. Each is linked with SENP2 in more than 1 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, CCER1 grouped by SENP2-low versus SENP2-high in CNS.

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
CNSCCER1 →+0.016+5.754<.001.00231
CNSPRAMEF7 →+0.183+5.754<.001.00231
CNSPRAMEF5 →+0.459+5.754<.001.00231
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

CCER1 by SENP2 expression — CNS

Box plot of CCER1 in SENP2-low vs SENP2-high samples in CNS.

Explore this box plot interactively →

Exploration