FRS2

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

Across TCGA patient cohorts, FRS2 mutation is significantly associated with the total protein of many other genes, with 41 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FRS2-associated genes across cancer lineages are FoxM1, MEK1, and mTOR_pS2448. Each is linked with FRS2 in more than 1 cancer types. Because this analysis shows association rather than direction, both FRS2-to-partner and partner-to-FRS2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FoxM1 grouped by FRS2-low versus FRS2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FRS2→partner) and Y-score (partner→FRS2) 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 →+0.238+1.765.014.01432
UCECMEK1 →+0.431+2.169.001.00332
UCECmTOR_pS2448 →-0.125-2.308.025.03332
UCECVEGFR2 →+0.357+2.676.001<.00132
UCECCaspase-7-cleavedD198 →+0.721+2.584.001.01032
UCECC-Raf →+0.234+1.765<.001.01432
Each partner links to its Q-omics profile. Showing the 6 strongest of 41 associations by consensus.

FoxM1 by FRS2 expression — UCEC

Box plot of FoxM1 in FRS2-low vs FRS2-high samples in UCEC.

Explore this box plot interactively →

Exploration