SPTBN5

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

Across TCGA patient cohorts, SPTBN5 mutation is significantly associated with the RNA expression of many other genes, with 7,003 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPTBN5-associated genes across cancer lineages are ZNF695, GRPEL1, and EIF2S1. Each is linked with SPTBN5 in more than 4 cancer types. Because this analysis shows association rather than direction, both SPTBN5-to-partner and partner-to-SPTBN5 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ZNF695 grouped by SPTBN5-low versus SPTBN5-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPTBN5→partner) and Y-score (partner→SPTBN5) 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
CESCZNF695 →+0.703+2.614.001.00535
UCECGRPEL1 →+0.419+1.925<.001<.00135
UCECEIF2S1 →+0.514+1.617<.001<.00135
STADIER3IP1 →+0.541+3.476<.001.00235
UCECOIP5 →+0.805+2.072<.001<.00135
UCECKNSTRN →+0.519+1.983<.001<.00135
Each partner links to its Q-omics profile. Showing the 6 strongest of 7,003 associations by consensus.

ZNF695 by SPTBN5 expression — CESC

Box plot of ZNF695 in SPTBN5-low vs SPTBN5-high samples in CESC.

Explore this box plot interactively →

Exploration