SHLD2

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

Across TCGA patient cohorts, SHLD2 mutation is significantly associated with the RNA expression of many other genes, with 4,092 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SHLD2-associated genes across cancer lineages are CCDC15, PTS, and EXOG. Each is linked with SHLD2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SHLD2-to-partner and partner-to-SHLD2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CCDC15 grouped by SHLD2-low versus SHLD2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SHLD2→partner) and Y-score (partner→SHLD2) 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
UCECCCDC15 →+0.485+2.906<.001<.00132
UCECPTS →+0.422+2.392<.001<.00132
UCECEXOG →+0.507+2.874<.001<.00132
UCECRER1 →+0.234+3.491.009.00232
UCECWNT4 →-0.728-3.786.001<.00132
UCECKIAA1841 →+0.459+3.880.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,092 associations by consensus.

CCDC15 by SHLD2 expression — UCEC

Box plot of CCDC15 in SHLD2-low vs SHLD2-high samples in UCEC.

Explore this box plot interactively →

Exploration