SPECC1L

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

Across TCGA cell cohorts, SPECC1L mutation is significantly associated with the drug of many other genes, with 31 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SPECC1L-associated genes across cancer lineages are Veliparib, Mirin, and Niraparib. Each is linked with SPECC1L in more than 1 cancer types. Because this analysis shows association rather than direction, both SPECC1L-to-partner and partner-to-SPECC1L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Veliparib grouped by SPECC1L-low versus SPECC1L-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPECC1L→partner) and Y-score (partner→SPECC1L) 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_INTESTINEVeliparib →+0.288+2.807.032.04631
LARGE_INTESTINEMirin →+0.382+2.807.025.03731
LARGE_INTESTINENiraparib →+0.416+2.700.009.03031
LARGE_INTESTINEN24798-49-A1 →+0.234+2.807.045.04531
LARGE_INTESTINEGSK2801 →+0.396+3.064.005.00931
LARGE_INTESTINEAGI-6780 →+0.349+3.061.047.01031
Each partner links to its Q-omics profile. Showing the 6 strongest of 31 associations by consensus.

Veliparib by SPECC1L expression — LARGE_INTESTINE

Box plot of Veliparib in SPECC1L-low vs SPECC1L-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration