FANCI

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

Across TCGA patient cohorts, FANCI mutation is significantly associated with the RNA expression of many other genes, with 5,014 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FANCI-associated genes across cancer lineages are RN7SL578P, MIR7976, and PLEKHJ1. Each is linked with FANCI in more than 2 cancer types. Because this analysis shows association rather than direction, both FANCI-to-partner and partner-to-FANCI results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL578P grouped by FANCI-low versus FANCI-high in READ.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FANCI→partner) and Y-score (partner→FANCI) 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
READRN7SL578P →+0.172+5.039<.001.00833
CESCMIR7976 →+0.915+4.269<.001.00333
UCECPLEKHJ1 →+0.687+2.470<.001<.00133
UCECPLEKHA8 →+0.409+3.201<.001<.00133
UCECPARP2 →+0.472+1.954<.001<.00133
UCECLSM4 →+0.367+2.192.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,014 associations by consensus.

RN7SL578P by FANCI expression — READ

Box plot of RN7SL578P in FANCI-low vs FANCI-high samples in READ.

Explore this box plot interactively →

Exploration