FCRLA

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

Across TCGA patient cohorts, FCRLA mutation is significantly associated with the RNA expression of many other genes, with 850 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FCRLA-associated genes across cancer lineages are HMGN1P32, MIR30B, and LSS. Each is linked with FCRLA in more than 2 cancer types. Because this analysis shows association rather than direction, both FCRLA-to-partner and partner-to-FCRLA results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, HMGN1P32 grouped by FCRLA-low versus FCRLA-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FCRLA→partner) and Y-score (partner→FCRLA) 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
UCECHMGN1P32 →+0.122+2.582.007.00333
STADMIR30B →+0.597+3.741<.001.00333
UCECLSS →+0.577+2.513.001.00932
UCECPTH1R →-0.805-2.896.007.00232
UCECTOP3A →+0.559+3.753<.001<.00132
UCECATP6V0A1 →+0.480+3.364.001.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 850 associations by consensus.

HMGN1P32 by FCRLA expression — UCEC

Box plot of HMGN1P32 in FCRLA-low vs FCRLA-high samples in UCEC.

Explore this box plot interactively →

Exploration