FRG1BP

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

Across TCGA patient cohorts, FRG1BP mutation is significantly associated with the RNA expression of many other genes, with 329 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FRG1BP-associated genes across cancer lineages are IFNA1, IFNA11P, and LINC01995. Each is linked with FRG1BP in more than 1 cancer types. Because this analysis shows association rather than direction, both FRG1BP-to-partner and partner-to-FRG1BP results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, IFNA1 grouped by FRG1BP-low versus FRG1BP-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FRG1BP→partner) and Y-score (partner→FRG1BP) 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
COADIFNA1 →+0.290+4.681<.001.00331
COADIFNA11P →+0.268+5.003<.001.00431
COADLINC01995 →+0.250+5.003<.001.00431
COADMIR6777 →+1.148+4.354.003.00731
HNSCTTTY2 →+0.014+7.954<.001.00831
UCECCASTOR2 →+1.124+3.191<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 329 associations by consensus.

IFNA1 by FRG1BP expression — COAD

Box plot of IFNA1 in FRG1BP-low vs FRG1BP-high samples in COAD.

Explore this box plot interactively →

Exploration