SAMSN1

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

Across TCGA patient cohorts, SAMSN1 mutation is significantly associated with the RNA expression of many other genes, with 3,759 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SAMSN1-associated genes across cancer lineages are RNA5SP161, RNU6-178P, and SPECC1P2. Each is linked with SAMSN1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SAMSN1-to-partner and partner-to-SAMSN1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNA5SP161 grouped by SAMSN1-low versus SAMSN1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SAMSN1→partner) and Y-score (partner→SAMSN1) 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
SKCMRNA5SP161 →+0.104+2.332.002.00433
BLCARNU6-178P →+0.599+4.167<.001.00432
LIHCSPECC1P2 →+0.438+6.676<.001<.00132
UCECMIR378H →+0.451+1.600.006.00532
HNSCAQP7P4 →+0.077+6.111<.001.00232
UCECPANK4 →+0.451+3.069<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,759 associations by consensus.

RNA5SP161 by SAMSN1 expression — SKCM

Box plot of RNA5SP161 in SAMSN1-low vs SAMSN1-high samples in SKCM.

Explore this box plot interactively →

Exploration