SFI1

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

Across TCGA cell cohorts, SFI1 mutation is significantly associated with the RNA expression of many other genes, with 330 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SFI1-associated genes across cancer lineages are MYO5B, KRTAP10-12, and LORICRIN. Each is linked with SFI1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SFI1-to-partner and partner-to-SFI1 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SFI1→partner) and Y-score (partner→SFI1) 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_INTESTINEMYO5B →+1.040+3.502.003.00132
SOFT_TISSUEKRTAP10-12 →+0.045+5.369<.001.00431
SOFT_TISSUELORICRIN →+0.021+4.930<.001.00831
SOFT_TISSUEOR10G4 →+0.048+4.930<.001.00831
KIDNEYC11orf53 →+0.033+5.000<.001.00531
KIDNEYGPR33 →+0.023+5.000<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 330 associations by consensus.

Exploration