SNORD115-38

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

Across TCGA patient cohorts, SNORD115-38 mutation is significantly associated with the RNA expression of many other genes, with 7 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNORD115-38-associated genes across cancer lineages are RBM17P2, MIR5003, and OR51C1P. Each is linked with SNORD115-38 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORD115-38-to-partner and partner-to-SNORD115-38 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 (SNORD115-38→partner) and Y-score (partner→SNORD115-38) 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
UCECRBM17P2 →+0.065+6.027.001.00231
UCECMIR5003 →+0.626+5.133<.001.00831
UCECOR51C1P →+0.094+5.420.004.00531
UCECMIR361 →+0.445+5.420.002.00531
UCECRNU6-1233P →+0.648+6.722.002<.00131
UCECMIR1255B2 →+1.309+6.335<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 7 associations by consensus.

Exploration