FBXW8

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

Across TCGA patient cohorts, FBXW8 mutation is significantly associated with the RNA expression of many other genes, with 1,294 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FBXW8-associated genes across cancer lineages are RNU4-26P, FAM30C, and RPS12P15. Each is linked with FBXW8 in more than 1 cancer types. Because this analysis shows association rather than direction, both FBXW8-to-partner and partner-to-FBXW8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU4-26P grouped by FBXW8-low versus FBXW8-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FBXW8→partner) and Y-score (partner→FBXW8) 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
HNSCRNU4-26P →+0.268+7.954<.001.00832
CESCFAM30C →+0.083+6.569<.001.00132
SKCMRPS12P15 →+0.073+2.591<.001.00432
UCECABHD3 →+0.819+3.180<.001<.00132
UCECEDA →-0.801-3.676<.001.00132
UCECLRR1 →+0.608+3.345.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,294 associations by consensus.

RNU4-26P by FBXW8 expression — HNSC

Box plot of RNU4-26P in FBXW8-low vs FBXW8-high samples in HNSC.

Explore this box plot interactively →

Exploration