FXR2

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

Across TCGA patient cohorts, FXR2 mutation is significantly associated with the RNA expression of many other genes, with 1,098 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FXR2-associated genes across cancer lineages are RNU1-62P, PRELID3BP1, and HMGB3P3. Each is linked with FXR2 in more than 1 cancer types. Because this analysis shows association rather than direction, both FXR2-to-partner and partner-to-FXR2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU1-62P grouped by FXR2-low versus FXR2-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FXR2→partner) and Y-score (partner→FXR2) 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
SKCMRNU1-62P →+0.164+4.282<.001.00932
SKCMPRELID3BP1 →+0.208+4.402<.001.00232
UCECHMGB3P3 →+0.151+2.021<.001.00132
BRCARNA5SP463 →+0.300+3.928<.001.00232
BRCACOMMD4P2 →+0.069+3.726.004.00532
BRCAMIR8061 →+0.224+4.215<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,098 associations by consensus.

RNU1-62P by FXR2 expression — SKCM

Box plot of RNU1-62P in FXR2-low vs FXR2-high samples in SKCM.

Explore this box plot interactively →

Exploration