SNORD116-28

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

Across TCGA patient cohorts, SNORD116-28 mutation is significantly associated with the RNA expression of many other genes, with 4 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SNORD116-28-associated genes across cancer lineages are RNU6-281P, OFD1P11Y, and MIR3152. Each is linked with SNORD116-28 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORD116-28-to-partner and partner-to-SNORD116-28 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-281P grouped by SNORD116-28-low versus SNORD116-28-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNORD116-28→partner) and Y-score (partner→SNORD116-28) 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
SKCMRNU6-281P →+0.373+7.816<.001.00831
SKCMOFD1P11Y →+0.039+7.816<.001.00831
SKCMMIR3152 →+0.478+7.816<.001.00831
SKCMMRPS5P4 →+0.139+7.816<.001.00831
Each partner links to its Q-omics profile. Showing the 4 strongest of 4 associations by consensus.

RNU6-281P by SNORD116-28 expression — SKCM

Box plot of RNU6-281P in SNORD116-28-low vs SNORD116-28-high samples in SKCM.

Explore this box plot interactively →

Exploration