SEMG1

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

Across TCGA patient cohorts, SEMG1 mutation is significantly associated with the RNA expression of many other genes, with 1,138 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SEMG1-associated genes across cancer lineages are RNA5SP297, SAP18P1, and NDUFA4P2. Each is linked with SEMG1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SEMG1-to-partner and partner-to-SEMG1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNA5SP297 grouped by SEMG1-low versus SEMG1-high in GBM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SEMG1→partner) and Y-score (partner→SEMG1) 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
GBMRNA5SP297 →+0.377+4.584<.001.00733
BRCASAP18P1 →+0.155+5.442<.001.00233
SKCMNDUFA4P2 →+0.048+1.978.002.00533
GBMMIR548AW →+0.655+4.584<.001.00732
GBMMIR4696 →+0.548+4.857<.001.00532
BRCAMIR6737 →+0.351+4.506<.001.00932
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,138 associations by consensus.

RNA5SP297 by SEMG1 expression — GBM

Box plot of RNA5SP297 in SEMG1-low vs SEMG1-high samples in GBM.

Explore this box plot interactively →

Exploration