FSCB

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

Across TCGA patient cohorts, FSCB mutation is significantly associated with the RNA expression of many other genes, with 6,870 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FSCB-associated genes across cancer lineages are C2orf49, POLE2, and GINS1. Each is linked with FSCB in more than 4 cancer types. Because this analysis shows association rather than direction, both FSCB-to-partner and partner-to-FSCB results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FSCB→partner) and Y-score (partner→FSCB) 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
LUSCC2orf49 →+0.282+1.877<.001.00135
UCECPOLE2 →+0.560+1.828<.001<.00134
UCECGINS1 →+0.576+1.321<.001.00234
UCECRAD51AP1 →+0.628+1.649<.001<.00134
UCECFANCE →+0.475+4.108<.001<.00134
UCECCENPA →+0.461+2.016.006<.00134
Each partner links to its Q-omics profile. Showing the 6 strongest of 6,870 associations by consensus.

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