SCN5A

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

Across TCGA patient cohorts, SCN5A mutation is significantly associated with the RNA expression of many other genes, with 7,885 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SCN5A-associated genes across cancer lineages are NDUFB6, SAAL1, and FBXO22. Each is linked with SCN5A in more than 4 cancer types. Because this analysis shows association rather than direction, both SCN5A-to-partner and partner-to-SCN5A results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SCN5A→partner) and Y-score (partner→SCN5A) 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
STADNDUFB6 →+0.377+1.973.007.00835
STADSAAL1 →+0.493+1.923<.001.00935
UCECFBXO22 →+0.436+1.672<.001<.00135
COADTIMM21 →+0.454+1.645<.001<.00135
UCECKIF18A →+0.423+1.136<.001<.00135
UCECAUNIP →+0.501+1.971<.001<.00135
Each partner links to its Q-omics profile. Showing the 6 strongest of 7,885 associations by consensus.

Exploration