RPS26

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

Across TCGA patient cohorts, RPS26 mutation is significantly associated with the RNA expression of many other genes, with 11 significant associations in total. BLCA shows the largest number of these associations.

The most reproducible RPS26-associated genes across cancer lineages are BCAR1P2, RN7SL66P, and SCGB1C2. Each is linked with RPS26 in more than 1 cancer types. Because this analysis shows association rather than direction, both RPS26-to-partner and partner-to-RPS26 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RPS26→partner) and Y-score (partner→RPS26) 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
BLCABCAR1P2 →+0.066+5.788<.001.00331
BLCARN7SL66P →+0.160+5.177<.001.00731
BLCASCGB1C2 →+0.136+5.177<.001.00731
BLCAMIR6854 →+0.747+5.251<.001.00631
HNSCRNU6-1159P →+0.403+7.954<.001.00831
HNSCPRAMEF29P →+0.039+7.954<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 11 associations by consensus.

Exploration