NAMPT

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

Across TCGA patient cohorts, NAMPT mutation is significantly associated with the RNA expression of many other genes, with 3,388 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NAMPT-associated genes across cancer lineages are SNORD32B, XAGE1A, and RNU6-679P. Each is linked with NAMPT in more than 1 cancer types. Because this analysis shows association rather than direction, both NAMPT-to-partner and partner-to-NAMPT results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNORD32B grouped by NAMPT-low versus NAMPT-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NAMPT→partner) and Y-score (partner→NAMPT) 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
HNSCSNORD32B →+0.420+6.357<.001<.00132
HNSCXAGE1A →+0.082+5.008<.001.00432
HNSCRNU6-679P →+0.350+5.763<.001.00132
BRCARNU6-374P →+0.142+8.057<.001.00532
LUADGAGE2A →+1.685+4.841<.001<.00132
HNSCLINC00564 →+0.268+5.339<.001.00332
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,388 associations by consensus.

SNORD32B by NAMPT expression — HNSC

Box plot of SNORD32B in NAMPT-low vs NAMPT-high samples in HNSC.

Explore this box plot interactively →

Exploration