FOLH1B

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

Across TCGA patient cohorts, FOLH1B mutation is significantly associated with the total protein of many other genes, with 57 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FOLH1B-associated genes across cancer lineages are FoxM1, Cyclin-E2, and Collagen-VI. Each is linked with FOLH1B in more than 3 cancer types. Because this analysis shows association rather than direction, both FOLH1B-to-partner and partner-to-FOLH1B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FoxM1 grouped by FOLH1B-low versus FOLH1B-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FOLH1B→partner) and Y-score (partner→FOLH1B) 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 →+0.249+2.070.005.00134
COADCyclin-E2 →+0.787+2.832<.001.03434
LUSCCollagen-VI →-0.326-3.450.014.00533
COADTFRC →+0.628+3.025.022.01933
UCECASNS →+0.323+2.321.009.00533
COADATM →-0.738-2.991<.001.03633
Each partner links to its Q-omics profile. Showing the 6 strongest of 57 associations by consensus.

FoxM1 by FOLH1B expression — UCEC

Box plot of FoxM1 in FOLH1B-low vs FOLH1B-high samples in UCEC.

Explore this box plot interactively →

Exploration