NAPSB

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

Across TCGA patient cohorts, NAPSB mutation is significantly associated with the RNA expression of many other genes, with 282 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NAPSB-associated genes across cancer lineages are TRAJ20, RN7SL643P, and SAR1B. Each is linked with NAPSB in more than 1 cancer types. Because this analysis shows association rather than direction, both NAPSB-to-partner and partner-to-NAPSB results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TRAJ20 grouped by NAPSB-low versus NAPSB-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NAPSB→partner) and Y-score (partner→NAPSB) 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
SKCMTRAJ20 →+0.433+3.425.002.00332
HNSCRN7SL643P →+0.110+4.655.003.00732
UCECSAR1B →+0.537+3.265.004.00831
UCECCPS1 →+0.811+3.523.002.00231
UCECMAPK9 →+0.500+3.201.003.00931
UCECLAG3 →+1.347+3.459<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 282 associations by consensus.

TRAJ20 by NAPSB expression — SKCM

Box plot of TRAJ20 in NAPSB-low vs NAPSB-high samples in SKCM.

Explore this box plot interactively →

Exploration