CSN3

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

Across TCGA patient cohorts, CSN3 mutation is significantly associated with the RNA expression of many other genes, with 474 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CSN3-associated genes across cancer lineages are FRG2, RNA5SP432, and MTHFD2P5. Each is linked with CSN3 in more than 1 cancer types. Because this analysis shows association rather than direction, both CSN3-to-partner and partner-to-CSN3 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FRG2 grouped by CSN3-low versus CSN3-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CSN3→partner) and Y-score (partner→CSN3) 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
COADFRG2 →+0.045+5.283.006.00632
LUADRNA5SP432 →+0.427+6.473<.001<.00132
LUADMTHFD2P5 →+0.124+4.722<.001.00332
LUADRPS20P25 →+0.081+4.712<.001.00732
LUADRNU6-299P →+0.264+4.631.009.00832
LUADCYP3A137P →+0.370+6.599<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 474 associations by consensus.

FRG2 by CSN3 expression — COAD

Box plot of FRG2 in CSN3-low vs CSN3-high samples in COAD.

Explore this box plot interactively →

Exploration