STN1

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

Across TCGA patient cohorts, STN1 mutation is significantly associated with the RNA expression of many other genes, with 915 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible STN1-associated genes across cancer lineages are MIR4276, RNU6-1318P, and CDH12P1. Each is linked with STN1 in more than 1 cancer types. Because this analysis shows association rather than direction, both STN1-to-partner and partner-to-STN1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR4276 grouped by STN1-low versus STN1-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (STN1→partner) and Y-score (partner→STN1) 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
HNSCMIR4276 →+0.413+7.954<.001.00832
UCECRNU6-1318P →+0.372+2.899<.001.00332
STADCDH12P1 →+0.094+5.105<.001.00832
BRCAH3P46 →+0.193+7.731<.001.00931
BRCAMIR3689D2 →+0.552+8.055<.001.00731
UCECSERPING1 →-0.839-3.807.008<.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 915 associations by consensus.

MIR4276 by STN1 expression — HNSC

Box plot of MIR4276 in STN1-low vs STN1-high samples in HNSC.

Explore this box plot interactively →

Exploration