SPTLC2

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

Across TCGA cell cohorts, SPTLC2 mutation is significantly associated with the RNA expression of many other genes, with 5 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SPTLC2-associated genes across cancer lineages are ACSM6, SMIM23, and IQCF5. 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, ACSM6 grouped by SPTLC2-low versus SPTLC2-high in LARGE_INTESTINE.

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
LARGE_INTESTINEACSM6 →+0.019+3.000.001.00531
BLOOD_LeukemiaSMIM23 →+0.030+6.569<.001<.00131
BLOOD_LeukemiaIQCF5 →+0.121+5.201<.001.00631
LARGE_INTESTINEC9orf153 →+0.232+3.497<.001.00421
LARGE_INTESTINETBR1 →+0.037+3.555.001.00311
Each partner links to its Q-omics profile. Showing the 5 strongest of 5 associations by consensus.

ACSM6 by SPTLC2 expression — LARGE_INTESTINE

Box plot of ACSM6 in SPTLC2-low vs SPTLC2-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration