OPN1SW

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

Across TCGA patient cohorts, OPN1SW mutation is significantly associated with the RNA expression of many other genes, with 533 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible OPN1SW-associated genes across cancer lineages are FGF12-AS1, RN7SL634P, and SUMO2P7. Each is linked with OPN1SW in more than 1 cancer types. Because this analysis shows association rather than direction, both OPN1SW-to-partner and partner-to-OPN1SW results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FGF12-AS1 grouped by OPN1SW-low versus OPN1SW-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (OPN1SW→partner) and Y-score (partner→OPN1SW) 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
SKCMFGF12-AS1 →+0.077+3.578.004.00732
COADRN7SL634P →+0.197+3.730.006.00432
UCECSUMO2P7 →+0.231+1.932.003<.00132
SKCMHSBP1P1 →+0.361+3.915<.001.00232
SKCMOR10K2 →+0.041+4.328<.001.00731
SKCMSERPINA13P →+0.018+4.199<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 533 associations by consensus.

FGF12-AS1 by OPN1SW expression — SKCM

Box plot of FGF12-AS1 in OPN1SW-low vs OPN1SW-high samples in SKCM.

Explore this box plot interactively →

Exploration