FBXL21P

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

Across TCGA patient cohorts, FBXL21P mutation is significantly associated with the RNA expression of many other genes, with 2,791 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FBXL21P-associated genes across cancer lineages are SLC25A18P1, RN7SL210P, and SCARNA21B. Each is linked with FBXL21P in more than 1 cancer types. Because this analysis shows association rather than direction, both FBXL21P-to-partner and partner-to-FBXL21P results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SLC25A18P1 grouped by FBXL21P-low versus FBXL21P-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FBXL21P→partner) and Y-score (partner→FBXL21P) 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
SKCMSLC25A18P1 →+0.066+5.225<.001.00132
SKCMRN7SL210P →+0.085+3.625<.001.00432
READSCARNA21B →+0.292+5.039.009.00832
COADMIR4710 →+0.713+4.602<.001.00832
UCECCCDC116 →+0.209+2.168<.001.00932
UCECR3HCC1L →+0.375+2.095.002.00332
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,791 associations by consensus.

SLC25A18P1 by FBXL21P expression — SKCM

Box plot of SLC25A18P1 in FBXL21P-low vs FBXL21P-high samples in SKCM.

Explore this box plot interactively →

Exploration