NRK

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

Across TCGA patient cohorts, NRK mutation is significantly associated with the RNA expression of many other genes, with 5,153 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NRK-associated genes across cancer lineages are SORCS2, NDUFB6, and PBK. Each is linked with NRK in more than 5 cancer types. Because this analysis shows association rather than direction, both NRK-to-partner and partner-to-NRK results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SORCS2 grouped by NRK-low versus NRK-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NRK→partner) and Y-score (partner→NRK) 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
UCECSORCS2 →-0.460-1.461<.001<.00136
UCECNDUFB6 →+0.349+1.297<.001<.00134
STADPBK →+0.909+2.824.002.00134
UCECCENPU →+0.510+1.329<.001<.00134
UCECCHAF1B →+0.468+1.214<.001<.00134
UCECH2AZ1 →+0.521+1.884<.001<.00134
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,153 associations by consensus.

SORCS2 by NRK expression — UCEC

Box plot of SORCS2 in NRK-low vs NRK-high samples in UCEC.

Explore this box plot interactively →

Exploration