NXNL2

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

Across TCGA patient cohorts, NXNL2 mutation is significantly associated with the RNA expression of many other genes, with 26 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible NXNL2-associated genes across cancer lineages are TRAJ36, RNU6-247P, and RNU6-905P. Each is linked with NXNL2 in more than 1 cancer types. Because this analysis shows association rather than direction, both NXNL2-to-partner and partner-to-NXNL2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TRAJ36 grouped by NXNL2-low versus NXNL2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NXNL2→partner) and Y-score (partner→NXNL2) 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
UCECTRAJ36 →+1.222+4.606<.001.00431
SKCMRNU6-247P →+0.376+4.979.004.00931
SKCMRNU6-905P →+0.396+5.513<.001.00431
SKCMSC4MOP →+0.057+5.680.009.00331
SKCMRPL7P3 →+0.139+5.362<.001.00531
SKCMLINC01392 →+0.138+5.224<.001.00731
Each partner links to its Q-omics profile. Showing the 6 strongest of 26 associations by consensus.

TRAJ36 by NXNL2 expression — UCEC

Box plot of TRAJ36 in NXNL2-low vs NXNL2-high samples in UCEC.

Explore this box plot interactively →

Exploration