NCF1C

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

Across TCGA patient cohorts, NCF1C mutation is significantly associated with the RNA expression of many other genes, with 54 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NCF1C-associated genes across cancer lineages are GAPDHP56, SPDYE9, and RNA5SP534. Each is linked with NCF1C in more than 1 cancer types. Because this analysis shows association rather than direction, both NCF1C-to-partner and partner-to-NCF1C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, GAPDHP56 grouped by NCF1C-low versus NCF1C-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NCF1C→partner) and Y-score (partner→NCF1C) 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
COADGAPDHP56 →+0.153+5.602.001<.00132
UCECSPDYE9 →+0.007+4.242<.001.00632
UCECRNA5SP534 →+0.392+3.920<.001<.00131
UCECIKBKGP1 →+0.122+2.884.001.00631
UCECMIR6781 →+0.827+3.043<.001.00231
COADRNA5SP286 →+0.603+4.893<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 54 associations by consensus.

GAPDHP56 by NCF1C expression — COAD

Box plot of GAPDHP56 in NCF1C-low vs NCF1C-high samples in COAD.

Explore this box plot interactively →

Exploration