WSCD2

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

Across TCGA patient cohorts, WSCD2 mutation is significantly associated with the RNA expression of many other genes, with 5,308 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible WSCD2-associated genes across cancer lineages are FOXM1, PKN3, and STIP1. Each is linked with WSCD2 in more than 4 cancer types. Because this analysis shows association rather than direction, both WSCD2-to-partner and partner-to-WSCD2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FOXM1 grouped by WSCD2-low versus WSCD2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (WSCD2→partner) and Y-score (partner→WSCD2) 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
UCECFOXM1 →+0.665+3.042.001<.00135
UCECPKN3 →+0.600+1.868<.001<.00135
UCECSTIP1 →+0.398+1.483<.001.00735
LUADSTRN4 →+0.437+2.854.004.00134
LUADOGFOD2 →+0.259+2.878.006.00134
SKCMDDX55 →+0.535+2.006<.001<.00134
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,308 associations by consensus.

FOXM1 by WSCD2 expression — UCEC

Box plot of FOXM1 in WSCD2-low vs WSCD2-high samples in UCEC.

Explore this box plot interactively →

Exploration