SPRED2

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

Across TCGA patient cohorts, SPRED2 mutation is significantly associated with the total protein of many other genes, with 51 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPRED2-associated genes across cancer lineages are GAPDH, mTOR_pS2448, and c-Met_pY1235. Each is linked with SPRED2 in more than 2 cancer types. Because this analysis shows association rather than direction, both SPRED2-to-partner and partner-to-SPRED2 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 (SPRED2→partner) and Y-score (partner→SPRED2) 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
UCECGAPDH →+0.377+1.440.043.02433
UCECmTOR_pS2448 →-0.115-2.202.025.01033
UCECc-Met_pY1235 →+0.053+1.736.037.00733
SKCM14-3-3_epsilon →+0.182+2.186.003.03432
UCECEGFR_pY1068 →-0.308-2.938<.001<.00132
UCECMEK1 →+0.454+2.459<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 51 associations by consensus.

Exploration