SPRN

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

Across TCGA patient cohorts, SPRN mutation is significantly associated with the immune_cell of many other genes, with 2 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPRN-associated genes across cancer lineages are CD8+ naive T-cells and Th2 cells. Each is linked with SPRN in more than 1 cancer types. Because this analysis shows association rather than direction, both SPRN-to-partner and partner-to-SPRN results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPRN→partner) and Y-score (partner→SPRN) 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
UCECCD8+ naive T-cells →+0.034+2.839.014.03431
UCECTh2 cells →+0.357+3.321<.001.01031
Each partner links to its Q-omics profile. Showing the 2 strongest of 2 associations by consensus.

Exploration