TNFRSF19

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

Across TCGA patient cohorts, TNFRSF19 mutation is significantly associated with the RNA expression of many other genes, with 1,543 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible TNFRSF19-associated genes across cancer lineages are RN7SL478P, UHRF1, and CALHM6. Each is linked with TNFRSF19 in more than 1 cancer types. Because this analysis shows association rather than direction, both TNFRSF19-to-partner and partner-to-TNFRSF19 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL478P grouped by TNFRSF19-low versus TNFRSF19-high in READ.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (TNFRSF19→partner) and Y-score (partner→TNFRSF19) 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
READRN7SL478P →+0.216+5.219<.001.00632
UCECUHRF1 →+0.642+1.595.003.00632
UCECCALHM6 →+0.761+2.584.002.00132
UCECZNF79 →+0.371+1.874<.001.00232
UCECFICD →+0.406+1.914.001.00932
UCECRNU6-597P →+0.339+1.785.001.00332
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,543 associations by consensus.

RN7SL478P by TNFRSF19 expression — READ

Box plot of RN7SL478P in TNFRSF19-low vs TNFRSF19-high samples in READ.

Explore this box plot interactively →

Exploration