SCN2A

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

Across TCGA patient cohorts, SCN2A mutation is significantly associated with the RNA expression of many other genes, with 7,106 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SCN2A-associated genes across cancer lineages are PRC1, CCNA2, and OIP5. Each is linked with SCN2A in more than 5 cancer types. Because this analysis shows association rather than direction, both SCN2A-to-partner and partner-to-SCN2A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PRC1 grouped by SCN2A-low versus SCN2A-high in LUAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SCN2A→partner) and Y-score (partner→SCN2A) 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
LUADPRC1 →+0.686+3.807<.001<.00136
UCECCCNA2 →+0.659+1.534<.001<.00136
UCECOIP5 →+0.717+1.799<.001<.00135
UCECCCNB1 →+0.680+1.914<.001<.00135
COADSHROOM4 →-0.804-2.087<.001.00535
UCECPTTG1 →+0.521+1.289<.001<.00135
Each partner links to its Q-omics profile. Showing the 6 strongest of 7,106 associations by consensus.

PRC1 by SCN2A expression — LUAD

Box plot of PRC1 in SCN2A-low vs SCN2A-high samples in LUAD.

Explore this box plot interactively →

Exploration