NPVF

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

Across TCGA patient cohorts, NPVF mutation is significantly associated with the RNA expression of many other genes, with 297 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NPVF-associated genes across cancer lineages are RN7SL248P, EZH2P1, and RNA5SP300. Each is linked with NPVF in more than 1 cancer types. Because this analysis shows association rather than direction, both NPVF-to-partner and partner-to-NPVF results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL248P grouped by NPVF-low versus NPVF-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NPVF→partner) and Y-score (partner→NPVF) 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
UCECRN7SL248P →+0.112+4.137<.001<.00132
UCECEZH2P1 →+0.422+3.486<.001<.00132
BRCARNA5SP300 →+0.481+5.646<.001.00432
SKCMRNU6-433P →+0.351+4.495<.001.00732
SKCMRNU6-905P →+0.365+5.098<.001<.00132
BRCAMIR6853 →+0.242+8.057<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 297 associations by consensus.

RN7SL248P by NPVF expression — UCEC

Box plot of RN7SL248P in NPVF-low vs NPVF-high samples in UCEC.

Explore this box plot interactively →

Exploration