FSD1L

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

Across TCGA patient cohorts, FSD1L mutation is significantly associated with the RNA expression of many other genes, with 2,483 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FSD1L-associated genes across cancer lineages are TRAJ12, SNORD114-18, and RNU6-74P. Each is linked with FSD1L in more than 2 cancer types. Because this analysis shows association rather than direction, both FSD1L-to-partner and partner-to-FSD1L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TRAJ12 grouped by FSD1L-low versus FSD1L-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FSD1L→partner) and Y-score (partner→FSD1L) 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
CESCTRAJ12 →+0.599+4.193.002.00933
UCECSNORD114-18 →+0.406+2.977<.001<.00132
UCECRNU6-74P →+0.138+2.397.007.00932
UCECRPL22P14 →+0.087+2.203<.001.00432
COADRN7SL83P →+0.516+5.392<.001.00232
UCECRNA5SP418 →+0.695+2.162<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,483 associations by consensus.

TRAJ12 by FSD1L expression — CESC

Box plot of TRAJ12 in FSD1L-low vs FSD1L-high samples in CESC.

Explore this box plot interactively →

Exploration