SCNN1A

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

Across TCGA patient cohorts, SCNN1A mutation is significantly associated with the RNA expression of many other genes, with 2,254 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SCNN1A-associated genes across cancer lineages are NEDD8-MDP1, ETFA, and RPL23AP82. Each is linked with SCNN1A in more than 2 cancer types. Because this analysis shows association rather than direction, both SCNN1A-to-partner and partner-to-SCNN1A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NEDD8-MDP1 grouped by SCNN1A-low versus SCNN1A-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SCNN1A→partner) and Y-score (partner→SCNN1A) 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
UCECNEDD8-MDP1 →+0.303+3.184<.001<.00133
UCECETFA →+0.624+2.839<.001.00133
SKCMRPL23AP82 →+0.716+2.613<.001.00533
UCECLDHAP1 →+0.136+2.463<.001.00133
GBMMIR4537 →+0.743+5.352<.001.00532
SKCMRNU6-762P →+0.554+2.610.007.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,254 associations by consensus.

NEDD8-MDP1 by SCNN1A expression — UCEC

Box plot of NEDD8-MDP1 in SCNN1A-low vs SCNN1A-high samples in UCEC.

Explore this box plot interactively →

Exploration