SNORD115-8

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

Across TCGA patient cohorts, SNORD115-8 mutation is significantly associated with the RNA expression of many other genes, with 33 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SNORD115-8-associated genes across cancer lineages are MIR8061, GEMIN2P1, and MMEL1-AS1. Each is linked with SNORD115-8 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORD115-8-to-partner and partner-to-SNORD115-8 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 (SNORD115-8→partner) and Y-score (partner→SNORD115-8) 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
SKCMMIR8061 →+0.664+7.219<.001<.00131
SKCMGEMIN2P1 →+0.058+5.292<.001.00631
SKCMMMEL1-AS1 →+0.292+5.594<.001.00431
SKCMLRRC7-AS1 →+0.187+6.199<.001.00131
SKCMOR7E117P →+0.071+5.771<.001.00331
SKCMRN7SL675P →+0.156+6.080<.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 33 associations by consensus.

Exploration