NARF

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

Across TCGA cell cohorts, NARF mutation is significantly associated with the RNA expression of many other genes, with 16 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible NARF-associated genes across cancer lineages are BVES, SULT6B1, and CLEC4F. Each is linked with NARF in more than 1 cancer types. Because this analysis shows association rather than direction, both NARF-to-partner and partner-to-NARF results are reported.

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

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NARF→partner) and Y-score (partner→NARF) 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
LARGE_INTESTINEBVES →+0.402+3.355.007.00731
LARGE_INTESTINESULT6B1 →+0.027+3.562<.001.00231
LARGE_INTESTINECLEC4F →+0.212+3.974.003.00231
LARGE_INTESTINEGJD2 →+0.002+3.700<.001.00931
LARGE_INTESTINEGFRA2 →+0.045+3.665<.001.00431
LARGE_INTESTINECPN2 →+0.046+4.714.008<.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 16 associations by consensus.

BVES by NARF expression — LARGE_INTESTINE

Box plot of BVES in NARF-low vs NARF-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration