SNTA1

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

Across TCGA patient cohorts, SNTA1 mutation is significantly associated with the RNA expression of many other genes, with 411 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNTA1-associated genes across cancer lineages are RNU6-73P, TXN2, and RN7SKP227. Each is linked with SNTA1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SNTA1-to-partner and partner-to-SNTA1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-73P grouped by SNTA1-low versus SNTA1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNTA1→partner) and Y-score (partner→SNTA1) 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
UCECRNU6-73P →+0.197+3.489.001.00333
UCECTXN2 →+0.416+2.556.004.00932
CESCRN7SKP227 →+0.073+4.144<.001.00932
CESCTRAJ12 →+0.632+3.608<.001.00432
BLCARNU6-141P →+0.705+4.216<.001.00332
CESCSMARCE1P2 →+0.090+4.129<.001.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 411 associations by consensus.

RNU6-73P by SNTA1 expression — UCEC

Box plot of RNU6-73P in SNTA1-low vs SNTA1-high samples in UCEC.

Explore this box plot interactively →

Exploration