NUP88

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

Across TCGA patient cohorts, NUP88 mutation is significantly associated with the RNA expression of many other genes, with 1,712 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NUP88-associated genes across cancer lineages are DEFB103A, PINCR, and RSL24D1P4. Each is linked with NUP88 in more than 1 cancer types. Because this analysis shows association rather than direction, both NUP88-to-partner and partner-to-NUP88 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, DEFB103A grouped by NUP88-low versus NUP88-high in LGG.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NUP88→partner) and Y-score (partner→NUP88) 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
LGGDEFB103A →+0.094+7.977<.001.00732
COADPINCR →+0.370+3.383<.001.00232
BLCARSL24D1P4 →+0.053+5.307<.001.00132
UCECMTHFD1 →+0.534+2.928<.001<.00132
UCECOIP5 →+0.755+3.000<.001<.00132
UCECR3HCC1 →+0.400+2.914.003.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,712 associations by consensus.

DEFB103A by NUP88 expression — LGG

Box plot of DEFB103A in NUP88-low vs NUP88-high samples in LGG.

Explore this box plot interactively →

Exploration