RASL11B

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

Across TCGA patient cohorts, RASL11B mutation is significantly associated with the RNA expression of many other genes, with 721 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RASL11B-associated genes across cancer lineages are HMGN1P34, RPL31P53, and RBMY2DP. Each is linked with RASL11B in more than 1 cancer types. Because this analysis shows association rather than direction, both RASL11B-to-partner and partner-to-RASL11B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, HMGN1P34 grouped by RASL11B-low versus RASL11B-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RASL11B→partner) and Y-score (partner→RASL11B) 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
BLCAHMGN1P34 →+0.175+4.433<.001.00732
BLCARPL31P53 →+0.078+4.562<.001.00632
BRCARBMY2DP →+0.029+9.057<.001.00332
SKCMRNU6-491P →+0.323+7.816<.001.00832
BRCAMIR6082 →+0.281+8.471<.001.00531
BLCASLC29A4P2 →+0.024+5.033<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 721 associations by consensus.

HMGN1P34 by RASL11B expression — BLCA

Box plot of HMGN1P34 in RASL11B-low vs RASL11B-high samples in BLCA.

Explore this box plot interactively →

Exploration