TNFSF13B

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

Across TCGA patient cohorts, TNFSF13B mutation is significantly associated with the RNA expression of many other genes, with 876 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible TNFSF13B-associated genes across cancer lineages are RN7SKP245, BOD1P1, and H4C7. Each is linked with TNFSF13B in more than 1 cancer types. Because this analysis shows association rather than direction, both TNFSF13B-to-partner and partner-to-TNFSF13B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SKP245 grouped by TNFSF13B-low versus TNFSF13B-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (TNFSF13B→partner) and Y-score (partner→TNFSF13B) 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
CESCRN7SKP245 →+0.130+5.812<.001.00332
SKCMBOD1P1 →+0.138+5.402<.001.00132
UCECH4C7 →+0.194+1.961<.001.00932
CESCRNA5SP75 →+0.309+5.103.007.00831
CESCTLE7 →+0.050+5.010.008.00931
CESCATP5MGP7 →+0.220+5.812<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 876 associations by consensus.

RN7SKP245 by TNFSF13B expression — CESC

Box plot of RN7SKP245 in TNFSF13B-low vs TNFSF13B-high samples in CESC.

Explore this box plot interactively →

Exploration