SNORD116-29

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

Across TCGA patient cohorts, SNORD116-29 mutation is significantly associated with the RNA expression of many other genes, with 38 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SNORD116-29-associated genes across cancer lineages are RNU4-64P, CAMTA1-AS2, and RNU7-54P. Each is linked with SNORD116-29 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORD116-29-to-partner and partner-to-SNORD116-29 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 (SNORD116-29→partner) and Y-score (partner→SNORD116-29) 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
SKCMRNU4-64P →+0.198+4.884<.001.00432
SKCMCAMTA1-AS2 →+0.071+4.402<.001.00231
SKCMRNU7-54P →+0.534+5.356<.001<.00131
SKCMRN7SL554P →+0.088+4.614<.001.00631
SKCMRN7SL813P →+0.101+4.385<.001.00831
SKCMMIR6839 →+0.205+5.408<.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 38 associations by consensus.

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