SNX4

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

Across TCGA patient cohorts, SNX4 mutation is significantly associated with the RNA expression of many other genes, with 2,323 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNX4-associated genes across cancer lineages are RNA5SP86, RNU6-281P, and RPS29P32. Each is linked with SNX4 in more than 2 cancer types. Because this analysis shows association rather than direction, both SNX4-to-partner and partner-to-SNX4 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNA5SP86 grouped by SNX4-low versus SNX4-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNX4→partner) and Y-score (partner→SNX4) 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
HNSCRNA5SP86 →+0.338+4.912<.001.00533
SKCMRNU6-281P →+0.373+7.816<.001.00832
HNSCRPS29P32 →+0.711+4.505<.001.00932
HNSCTAAR8 →+0.094+6.020<.001<.00132
HNSCOR5F2P →+0.240+4.578<.001.00832
HNSCRNU6-508P →+0.443+6.357<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,323 associations by consensus.

RNA5SP86 by SNX4 expression — HNSC

Box plot of RNA5SP86 in SNX4-low vs SNX4-high samples in HNSC.

Explore this box plot interactively →

Exploration