SNX10

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

Across TCGA patient cohorts, SNX10 mutation is significantly associated with the RNA expression of many other genes, with 264 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNX10-associated genes across cancer lineages are RNA5SP158, RN7SL722P, and RNA5SP94. Each is linked with SNX10 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNX10-to-partner and partner-to-SNX10 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNA5SP158 grouped by SNX10-low versus SNX10-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNX10→partner) and Y-score (partner→SNX10) 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
SKCMRNA5SP158 →+0.606+5.436<.001.00532
BRCARN7SL722P →+0.119+8.471<.001.00531
BRCARNA5SP94 →+0.276+7.731<.001.00931
BRCAYWHAEP2 →+0.269+9.057<.001.00331
UCECNDUFAF5 →+0.541+3.534<.001.00231
UCECPITRM1 →+0.683+3.459.002.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 264 associations by consensus.

RNA5SP158 by SNX10 expression — SKCM

Box plot of RNA5SP158 in SNX10-low vs SNX10-high samples in SKCM.

Explore this box plot interactively →

Exploration