SLFN12

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

Across TCGA patient cohorts, SLFN12 mutation is significantly associated with the total protein of many other genes, with 19 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLFN12-associated genes across cancer lineages are Stathmin, Chk2, and beta-Catenin. Each is linked with SLFN12 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLFN12-to-partner and partner-to-SLFN12 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Stathmin grouped by SLFN12-low versus SLFN12-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLFN12→partner) and Y-score (partner→SLFN12) 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
UCECStathmin →+0.150+2.115.012.01932
UCECChk2 →-0.252-2.807.013.00332
SKCMbeta-Catenin →-0.701-3.459.002.00532
SKCME-Cadherin →-0.932-2.000.017.03132
UCECEGFR_pY1068 →-0.271-2.807.013.00331
UCECMEK1 →+0.405+2.459.011.01931
Each partner links to its Q-omics profile. Showing the 6 strongest of 19 associations by consensus.

Stathmin by SLFN12 expression — UCEC

Box plot of Stathmin in SLFN12-low vs SLFN12-high samples in UCEC.

Explore this box plot interactively →

Exploration