NRK

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

Across TCGA patient cohorts, NRK mutation is significantly associated with the total protein of many other genes, with 70 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NRK-associated genes across cancer lineages are ASNS, 4E-BP1, and Smad1. Each is linked with NRK in more than 4 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, ASNS 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
UCECASNS →+0.208+0.725.010.03535
COAD4E-BP1 →+0.341+3.321<.001.00935
LUADSmad1 →+0.224+2.819<.001.03525
STADFoxM1 →+0.254+2.700.017.00534
COAD14-3-3_beta →-0.238-2.674.004.00633
LUSCp27 →-0.146-1.691.015.04333
Each partner links to its Q-omics profile. Showing the 6 strongest of 70 associations by consensus.

ASNS by NRK expression — UCEC

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

Explore this box plot interactively →

Exploration