FRRS1L

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

Across TCGA patient cohorts, FRRS1L mutation is significantly associated with the total protein of many other genes, with 4 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FRRS1L-associated genes across cancer lineages are ERK2, Annexin-1, and STAT5a. Each is linked with FRRS1L in more than 1 cancer types. Because this analysis shows association rather than direction, both FRRS1L-to-partner and partner-to-FRRS1L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ERK2 grouped by FRRS1L-low versus FRRS1L-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FRRS1L→partner) and Y-score (partner→FRRS1L) 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
UCECERK2 →+0.209+3.169.048.02031
UCECAnnexin-1 →+0.643+3.169.026.02012
UCECSTAT5a →+0.594+3.169.006.02011
UCECCD20 →+0.152+3.169.035.02011
Each partner links to its Q-omics profile. Showing the 4 strongest of 4 associations by consensus.

ERK2 by FRRS1L expression — UCEC

Box plot of ERK2 in FRRS1L-low vs FRRS1L-high samples in UCEC.

Explore this box plot interactively →

Exploration