TNFRSF10B

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

Across TCGA patient cohorts, TNFRSF10B mutation is significantly associated with the RNA expression of many other genes, with 1,191 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible TNFRSF10B-associated genes across cancer lineages are SLC20A1P3, MCOLN1, and SNHG30. Each is linked with TNFRSF10B in more than 2 cancer types. Because this analysis shows association rather than direction, both TNFRSF10B-to-partner and partner-to-TNFRSF10B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SLC20A1P3 grouped by TNFRSF10B-low versus TNFRSF10B-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (TNFRSF10B→partner) and Y-score (partner→TNFRSF10B) 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
COADSLC20A1P3 →+0.163+7.502<.001<.00133
UCECMCOLN1 →+0.517+2.415<.001.00332
UCECSNHG30 →+0.534+3.708.001<.00132
UCECNDUFA7 →+0.438+2.415.004.00332
UCECRPL23AP82 →+0.470+3.467<.001.00232
UCECLONP1 →+0.544+3.616.002.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,191 associations by consensus.

SLC20A1P3 by TNFRSF10B expression — COAD

Box plot of SLC20A1P3 in TNFRSF10B-low vs TNFRSF10B-high samples in COAD.

Explore this box plot interactively →

Exploration