SNORD108

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

Across TCGA patient cohorts, SNORD108 mutation is significantly associated with the RNA expression of many other genes, with 8 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SNORD108-associated genes across cancer lineages are LINC02479, RNU6-947P, and PRR23D2. Each is linked with SNORD108 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORD108-to-partner and partner-to-SNORD108 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, LINC02479 grouped by SNORD108-low versus SNORD108-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNORD108→partner) and Y-score (partner→SNORD108) 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
SKCMLINC02479 →+0.049+7.816<.001.00831
SKCMRNU6-947P →+0.258+7.816<.001.00831
SKCMPRR23D2 →+0.019+7.816<.001.00831
SKCMMIR3152 →+0.478+7.816<.001.00831
SKCMFAM32DP →+0.094+7.816<.001.00831
SKCMMRPS5P4 →+0.139+7.816<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 8 associations by consensus.

LINC02479 by SNORD108 expression — SKCM

Box plot of LINC02479 in SNORD108-low vs SNORD108-high samples in SKCM.

Explore this box plot interactively →

Exploration