NVL

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

Across TCGA patient cohorts, NVL mutation is significantly associated with the RNA expression of many other genes, with 4,696 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NVL-associated genes across cancer lineages are EIF4A2P5, RNA5SP333, and BUB3. Each is linked with NVL in more than 2 cancer types. Because this analysis shows association rather than direction, both NVL-to-partner and partner-to-NVL results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, EIF4A2P5 grouped by NVL-low versus NVL-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NVL→partner) and Y-score (partner→NVL) 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
SKCMEIF4A2P5 →+0.029+3.343<.001.00433
LUADRNA5SP333 →+0.226+4.303<.001.00933
UCECBUB3 →+0.593+2.584<.001<.00133
UCECELP6 →+0.247+2.024.006.00733
UCECRRP36 →+0.364+2.021<.001<.00133
KIRPRNA5SP426 →+0.284+5.159<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,696 associations by consensus.

EIF4A2P5 by NVL expression — SKCM

Box plot of EIF4A2P5 in NVL-low vs NVL-high samples in SKCM.

Explore this box plot interactively →

Exploration