SPTLC2

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

Across TCGA patient cohorts, SPTLC2 mutation is significantly associated with the total protein of many other genes, with 45 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPTLC2-associated genes across cancer lineages are eIF4E, INPP4B, and STAT5a. Each is linked with SPTLC2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SPTLC2-to-partner and partner-to-SPTLC2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, eIF4E grouped by SPTLC2-low versus SPTLC2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPTLC2→partner) and Y-score (partner→SPTLC2) 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
UCECeIF4E →+0.221+3.247.006<.00132
UCECINPP4B →-0.313-2.906.011.00132
UCECSTAT5a →+0.323+2.584.035.01032
UCECASNS →+0.667+3.000<.001<.00132
UCECCyclin-E2 →+0.175+2.087.006.00532
UCEC14-3-3_beta →-0.089-1.847.020.04931
Each partner links to its Q-omics profile. Showing the 6 strongest of 45 associations by consensus.

eIF4E by SPTLC2 expression — UCEC

Box plot of eIF4E in SPTLC2-low vs SPTLC2-high samples in UCEC.

Explore this box plot interactively →

Exploration