FCRL2

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

Across TCGA patient cohorts, FCRL2 mutation is significantly associated with the RNA expression of many other genes, with 3,732 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FCRL2-associated genes across cancer lineages are CHEK1, CHAF1B, and RACGAP1. Each is linked with FCRL2 in more than 2 cancer types. Because this analysis shows association rather than direction, both FCRL2-to-partner and partner-to-FCRL2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CHEK1 grouped by FCRL2-low versus FCRL2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FCRL2→partner) and Y-score (partner→FCRL2) 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
UCECCHEK1 →+0.695+2.606<.001<.00133
UCECCHAF1B →+0.547+2.679<.001<.00133
UCECRACGAP1 →+0.565+2.021.004.00533
UCECUSP39 →+0.324+2.839.002.00133
UCECPXMP2 →+0.576+2.016.001.00133
UCECRAD51 →+0.835+2.654<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,732 associations by consensus.

CHEK1 by FCRL2 expression — UCEC

Box plot of CHEK1 in FCRL2-low vs FCRL2-high samples in UCEC.

Explore this box plot interactively →

Exploration