SEPTIN8

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

Across TCGA patient cohorts, SEPTIN8 mutation is significantly associated with the RNA expression of many other genes, with 1,406 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SEPTIN8-associated genes across cancer lineages are RN7SL248P, RNU6-451P, and RN7SL470P. Each is linked with SEPTIN8 in more than 1 cancer types. Because this analysis shows association rather than direction, both SEPTIN8-to-partner and partner-to-SEPTIN8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL248P grouped by SEPTIN8-low versus SEPTIN8-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SEPTIN8→partner) and Y-score (partner→SEPTIN8) 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
UCECRN7SL248P →+0.059+3.137<.001.00532
UCECRNU6-451P →+0.339+2.123<.001.00932
UCECRN7SL470P →+0.182+1.993.001.00332
BLCARNU6-502P →+0.476+5.588<.001.00432
LUADRNU6-114P →+0.215+6.108<.001.00132
SKCMBANF1P5 →+0.179+3.287.001.00832
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,406 associations by consensus.

RN7SL248P by SEPTIN8 expression — UCEC

Box plot of RN7SL248P in SEPTIN8-low vs SEPTIN8-high samples in UCEC.

Explore this box plot interactively →

Exploration