FRRS1L

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

Across TCGA cell cohorts, FRRS1L mutation is significantly associated with the RNA expression of many other genes, with 7 significant associations in total. LUNG_SCLC shows the largest number of these associations.

The most reproducible FRRS1L-associated genes across cancer lineages are VN1R4, IL3, and PRAMEF10. 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, VN1R4 grouped by FRRS1L-low versus FRRS1L-high in CNS.

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
CNSVN1R4 →+0.098+5.754<.001.00231
LUNG_SCLCIL3 →+0.055+5.029<.001.00631
LUNG_SCLCPRAMEF10 →+1.180+5.643<.001.00231
LUNG_SCLCPRAMEF17 →+0.013+5.643<.001.00231
LUNG_SCLCSPINK8 →+0.513+5.029<.001.00631
LUNG_SCLCPRAMEF33 →+0.649+5.029<.001.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 7 associations by consensus.

VN1R4 by FRRS1L expression — CNS

Box plot of VN1R4 in FRRS1L-low vs FRRS1L-high samples in CNS.

Explore this box plot interactively →

Exploration