SLFN14

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

Across TCGA cell cohorts, SLFN14 mutation is significantly associated with the RNA expression of many other genes, with 2 significant associations in total. SKIN shows the largest number of these associations.

The most reproducible SLFN14-associated genes across cancer lineages are KRTAP10-4 and GPR142. Each is linked with SLFN14 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLFN14-to-partner and partner-to-SLFN14 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, KRTAP10-4 grouped by SLFN14-low versus SLFN14-high in SKIN.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLFN14→partner) and Y-score (partner→SLFN14) 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
SKINKRTAP10-4 →+0.015+5.022<.001.00231
SKINGPR142 →+0.019+4.930.002.00131
Each partner links to its Q-omics profile. Showing the 2 strongest of 2 associations by consensus.

KRTAP10-4 by SLFN14 expression — SKIN

Box plot of KRTAP10-4 in SLFN14-low vs SLFN14-high samples in SKIN.

Explore this box plot interactively →

Exploration