SPART

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

Across TCGA patient cohorts, SPART mutation is significantly associated with the total protein of many other genes, with 46 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPART-associated genes across cancer lineages are FASN, PDCD4, and Caspase-7-cleavedD198. Each is linked with SPART in more than 2 cancer types. Because this analysis shows association rather than direction, both SPART-to-partner and partner-to-SPART results are reported.

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

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPART→partner) and Y-score (partner→SPART) 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
STADFASN →+0.457+3.015.014.01833
STADPDCD4 →-0.526-3.459.008.00533
STADCaspase-7-cleavedD198 →+0.837+2.321.012.03433
STAD4E-BP1 →+0.368+3.169.006.01733
UCECPCNA →+0.194+2.700.008.00533
UCECATM →-0.372-1.794.016.02433
Each partner links to its Q-omics profile. Showing the 6 strongest of 46 associations by consensus.

FASN by SPART expression — STAD

Box plot of FASN in SPART-low vs SPART-high samples in STAD.

Explore this box plot interactively →

Exploration