SNX15

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

Across TCGA patient cohorts, SNX15 mutation is significantly associated with the RNA expression of many other genes, with 2,428 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNX15-associated genes across cancer lineages are RN7SL271P, FABP5P10, and RPL35AP19. Each is linked with SNX15 in more than 2 cancer types. Because this analysis shows association rather than direction, both SNX15-to-partner and partner-to-SNX15 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL271P grouped by SNX15-low versus SNX15-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNX15→partner) and Y-score (partner→SNX15) 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
BRCARN7SL271P →+0.091+5.365<.001.00233
COADFABP5P10 →+0.193+3.455.003<.00133
BRCARPL35AP19 →+0.141+4.331.006.00332
UCECRNA5SP414 →+0.691+2.255<.001.00932
UCECGEMIN4 →+0.800+3.807<.001<.00132
UCECCYB5D1 →+0.383+3.370.009.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,428 associations by consensus.

RN7SL271P by SNX15 expression — BRCA

Box plot of RN7SL271P in SNX15-low vs SNX15-high samples in BRCA.

Explore this box plot interactively →

Exploration