SNORD107

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

Across TCGA patient cohorts, SNORD107 mutation is significantly associated with the RNA expression of many other genes, with 213 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SNORD107-associated genes across cancer lineages are FABP12P1, LINC00709, and RN7SL387P. Each is linked with SNORD107 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORD107-to-partner and partner-to-SNORD107 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FABP12P1 grouped by SNORD107-low versus SNORD107-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNORD107→partner) and Y-score (partner→SNORD107) 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
SKCMFABP12P1 →+0.059+4.212<.001.00732
SKCMLINC00709 →+0.028+4.212.005.00732
SKCMRN7SL387P →+0.171+3.164<.001.00332
SKCMMIR4499 →+0.373+3.393.003.00132
SKCMMIR5682 →+0.201+4.634<.001.00332
SKCMOR4C11 →+0.018+5.225<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 213 associations by consensus.

FABP12P1 by SNORD107 expression — SKCM

Box plot of FABP12P1 in SNORD107-low vs SNORD107-high samples in SKCM.

Explore this box plot interactively →

Exploration