SNAI1

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

Across TCGA patient cohorts, SNAI1 mutation is significantly associated with the RNA expression of many other genes, with 178 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SNAI1-associated genes across cancer lineages are RNU105C, RN7SKP33, and LINC01802. Each is linked with SNAI1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SNAI1-to-partner and partner-to-SNAI1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU105C grouped by SNAI1-low versus SNAI1-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNAI1→partner) and Y-score (partner→SNAI1) 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
CESCRNU105C →+0.141+4.969.006.00433
SKCMRN7SKP33 →+0.058+4.634<.001.00332
SKCMLINC01802 →+0.417+4.199<.001<.00132
SKCMAKR1B10P2 →+0.038+5.225<.001.00132
UCECRNU6-1290P →+0.284+4.049<.001.00832
UCECFKBP14-AS1 →+0.337+3.223.007.00932
Each partner links to its Q-omics profile. Showing the 6 strongest of 178 associations by consensus.

RNU105C by SNAI1 expression — CESC

Box plot of RNU105C in SNAI1-low vs SNAI1-high samples in CESC.

Explore this box plot interactively →

Exploration