SPPL2B

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

Across TCGA patient cohorts, SPPL2B mutation is significantly associated with the RNA expression of many other genes, with 2,392 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPPL2B-associated genes across cancer lineages are KRT19P6, DTWD1, and BLOC1S6. Each is linked with SPPL2B in more than 2 cancer types. Because this analysis shows association rather than direction, both SPPL2B-to-partner and partner-to-SPPL2B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, KRT19P6 grouped by SPPL2B-low versus SPPL2B-high in LUSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPPL2B→partner) and Y-score (partner→SPPL2B) 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
LUSCKRT19P6 →+0.100+5.008<.001.00233
UCECDTWD1 →+0.348+2.831.002.00133
UCECBLOC1S6 →+0.562+2.403<.001<.00133
UCECGALNT7 →+0.728+2.021.001.00133
UCECKAT2B →+0.609+2.032<.001.00133
UCECBRCA1 →+0.514+2.392.004<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,392 associations by consensus.

KRT19P6 by SPPL2B expression — LUSC

Box plot of KRT19P6 in SPPL2B-low vs SPPL2B-high samples in LUSC.

Explore this box plot interactively →

Exploration