FRS2

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

Across TCGA patient cohorts, FRS2 mutation is significantly associated with the RNA expression of many other genes, with 3,450 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FRS2-associated genes across cancer lineages are MIR98, RNA5SP412, and RNU1-31P. 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, MIR98 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
UCECMIR98 →+0.187+1.863.002.00832
UCECRNA5SP412 →+0.471+1.815<.001.00232
CESCRNU1-31P →+0.454+4.669<.001.00732
CESCGAGE12H →+0.394+5.837<.001.00132
UCECRNU6-918P →+0.244+2.157<.001.00632
UCECRNA5SP415 →+0.361+2.096.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,450 associations by consensus.

MIR98 by FRS2 expression — UCEC

Box plot of MIR98 in FRS2-low vs FRS2-high samples in UCEC.

Explore this box plot interactively →

Exploration