STK38L

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

Across TCGA patient cohorts, STK38L mutation is significantly associated with the RNA expression of many other genes, with 1,700 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible STK38L-associated genes across cancer lineages are YTHDF3-AS1, RNU6-796P, and HMGB1P23. Each is linked with STK38L in more than 1 cancer types. Because this analysis shows association rather than direction, both STK38L-to-partner and partner-to-STK38L results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (STK38L→partner) and Y-score (partner→STK38L) 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
UCECYTHDF3-AS1 →+0.705+2.960<.001<.00132
HNSCRNU6-796P →+0.408+6.221<.001.00132
SKCMHMGB1P23 →+0.050+3.046.002.00432
HNSCCICP2 →+0.023+7.623<.001<.00132
UCECSNX3P1Y →+0.104+4.571<.001.00232
UCECRNA5SP502 →+0.534+2.824.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,700 associations by consensus.

Exploration