SV2A

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

Across TCGA patient cohorts, SV2A mutation is significantly associated with the total protein of many other genes, with 53 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SV2A-associated genes across cancer lineages are C-Raf, Cyclin-B1, and MEK1. Each is linked with SV2A in more than 3 cancer types. Because this analysis shows association rather than direction, both SV2A-to-partner and partner-to-SV2A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, C-Raf grouped by SV2A-low versus SV2A-high in STAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SV2A→partner) and Y-score (partner→SV2A) 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
STADC-Raf →+0.215+2.584.001.01034
UCECCyclin-B1 →+0.651+2.137<.001.00134
UCECMEK1 →+0.373+1.765.002.01333
UCEC4E-BP1 →+0.342+2.807<.001.00233
UCECKu80 →+0.339+2.920<.001<.00132
STADBRCA2 →-0.169-3.169.004.01732
Each partner links to its Q-omics profile. Showing the 6 strongest of 53 associations by consensus.

C-Raf by SV2A expression — STAD

Box plot of C-Raf in SV2A-low vs SV2A-high samples in STAD.

Explore this box plot interactively →

Exploration