SNORA22C

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

Across TCGA patient cohorts, SNORA22C mutation is significantly associated with the RNA expression of many other genes, with 1 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNORA22C-associated genes across cancer lineages are MIR4752. Each is linked with SNORA22C in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORA22C-to-partner and partner-to-SNORA22C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR4752 grouped by SNORA22C-low versus SNORA22C-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNORA22C→partner) and Y-score (partner→SNORA22C) 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
UCECMIR4752 →+0.618+8.066<.001.00731
Each partner links to its Q-omics profile. Showing the 1 strongest of 1 associations by consensus.

MIR4752 by SNORA22C expression — UCEC

Box plot of MIR4752 in SNORA22C-low vs SNORA22C-high samples in UCEC.

Explore this box plot interactively →

Exploration