FANCC

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

Across TCGA cell cohorts, FANCC mutation is significantly associated with the RNA expression of many other genes, with 4 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible FANCC-associated genes across cancer lineages are GFRA4, INSL5, and ABCG8. Each is linked with FANCC in more than 1 cancer types. Because this analysis shows association rather than direction, both FANCC-to-partner and partner-to-FANCC results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, GFRA4 grouped by FANCC-low versus FANCC-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FANCC→partner) and Y-score (partner→FANCC) 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_INTESTINEGFRA4 →+0.019+3.345.001.00731
LARGE_INTESTINEINSL5 →+0.376+3.626<.001.00631
LARGE_INTESTINEABCG8 →+0.377+3.453<.001.00921
LARGE_INTESTINEIL20 →+0.293+3.984<.001.00121
Each partner links to its Q-omics profile. Showing the 4 strongest of 4 associations by consensus.

GFRA4 by FANCC expression — LARGE_INTESTINE

Box plot of GFRA4 in FANCC-low vs FANCC-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration