SNX18

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

Across TCGA cell cohorts, SNX18 mutation is significantly associated with the RNA expression of many other genes, with 207 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SNX18-associated genes across cancer lineages are BRDT, BTBD16, and DIRAS2. Each is linked with SNX18 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNX18-to-partner and partner-to-SNX18 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, BRDT grouped by SNX18-low versus SNX18-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNX18→partner) and Y-score (partner→SNX18) 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
BLOOD_LeukemiaBRDT →+0.174+4.342<.001.00231
BLOOD_LeukemiaBTBD16 →+0.086+3.959<.001.00531
BLOOD_LeukemiaDIRAS2 →+0.055+4.087.008.00931
BLOOD_LeukemiaKRT6C →+0.017+4.037<.001.00431
BLOOD_LeukemiaTEX43 →+0.084+4.384<.001.00631
BLOOD_LeukemiaTEX35 →+0.198+3.769<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 207 associations by consensus.

BRDT by SNX18 expression — BLOOD_Leukemia

Box plot of BRDT in SNX18-low vs SNX18-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration