SHD

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

Across TCGA patient cohorts, SHD mutation is significantly associated with the total protein of many other genes, with 13 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SHD-associated genes across cancer lineages are FoxM1, Heregulin, and MAPK_pT202_Y204. Each is linked with SHD in more than 1 cancer types. Because this analysis shows association rather than direction, both SHD-to-partner and partner-to-SHD results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FoxM1 grouped by SHD-low versus SHD-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SHD→partner) and Y-score (partner→SHD) 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 →+0.298+2.817.021.03631
UCECHeregulin →-0.152-3.459.014.00531
UCECMAPK_pT202_Y204 →-0.475-2.321.044.03531
UCECp27_pT198 →+0.113+2.321.035.03531
UCECRab11 →-0.160-2.321.028.03531
UCECS6_pS240_S244 →+0.402+3.000.049.03631
Each partner links to its Q-omics profile. Showing the 6 strongest of 13 associations by consensus.

FoxM1 by SHD expression — UCEC

Box plot of FoxM1 in SHD-low vs SHD-high samples in UCEC.

Explore this box plot interactively →

Exploration