NRBF2

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

Across TCGA patient cohorts, NRBF2 mutation is significantly associated with the RNA expression of many other genes, with 1,951 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NRBF2-associated genes across cancer lineages are TRAJ5, OR9M1P, and SNORD37. Each is linked with NRBF2 in more than 1 cancer types. Because this analysis shows association rather than direction, both NRBF2-to-partner and partner-to-NRBF2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TRAJ5 grouped by NRBF2-low versus NRBF2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NRBF2→partner) and Y-score (partner→NRBF2) 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
UCECTRAJ5 →+0.513+1.680<.001.00232
COADOR9M1P →+0.057+5.409<.001.00131
COADSNORD37 →+1.180+3.711<.001.00731
COADRNU6-1127P →+0.308+4.721.002.00431
COADRNU6-136P →+0.377+3.636.004.00631
COADSDC4P →+0.123+4.283<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,951 associations by consensus.

TRAJ5 by NRBF2 expression — UCEC

Box plot of TRAJ5 in NRBF2-low vs NRBF2-high samples in UCEC.

Explore this box plot interactively →

Exploration