SMPDL3A

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

Across TCGA patient cohorts, SMPDL3A mutation is significantly associated with the RNA expression of many other genes, with 3,236 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SMPDL3A-associated genes across cancer lineages are NF1P10, RNA5SP413, and MIR4445. Each is linked with SMPDL3A in more than 1 cancer types. Because this analysis shows association rather than direction, both SMPDL3A-to-partner and partner-to-SMPDL3A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NF1P10 grouped by SMPDL3A-low versus SMPDL3A-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SMPDL3A→partner) and Y-score (partner→SMPDL3A) 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
CESCNF1P10 →+0.175+5.569<.001.00232
LUADRNA5SP413 →+0.274+7.930<.001.00832
UCECMIR4445 →+0.189+4.571<.001.00232
SKCMCDRT15P3 →+0.044+4.563.001.00432
SKCMOR6C65 →+0.036+5.797<.001.00132
SKCMRBPJP6 →+0.025+4.970<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,236 associations by consensus.

NF1P10 by SMPDL3A expression — CESC

Box plot of NF1P10 in SMPDL3A-low vs SMPDL3A-high samples in CESC.

Explore this box plot interactively →

Exploration