SLK

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

Across TCGA cell cohorts, SLK mutation is significantly associated with the RNA expression of many other genes, with 40 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLK-associated genes across cancer lineages are REG1B, TRIM49D2, and AVP. Each is linked with SLK in more than 1 cancer types. Because this analysis shows association rather than direction, both SLK-to-partner and partner-to-SLK results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, REG1B grouped by SLK-low versus SLK-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLK→partner) and Y-score (partner→SLK) 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
LARGE_INTESTINEREG1B →+2.366+2.518<.001.00632
STOMACHTRIM49D2 →+0.040+5.285<.001.00331
BLOOD_LymphomaAVP →+0.031+5.209<.001.00531
BLOOD_LymphomaCABP5 →+0.012+4.867<.001.00931
BLOOD_LymphomaDEFB129 →+0.043+6.247<.001<.00131
BLOOD_LymphomaREG3G →+0.040+4.867<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 40 associations by consensus.

REG1B by SLK expression — LARGE_INTESTINE

Box plot of REG1B in SLK-low vs SLK-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration