SYNCRIP

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

Across TCGA cell cohorts, SYNCRIP mutation is significantly associated with the RNA expression of many other genes, with 222 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SYNCRIP-associated genes across cancer lineages are CBY1, IFT27, and INTS10. Each is linked with SYNCRIP in more than 1 cancer types. Because this analysis shows association rather than direction, both SYNCRIP-to-partner and partner-to-SYNCRIP results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CBY1 grouped by SYNCRIP-low versus SYNCRIP-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SYNCRIP→partner) and Y-score (partner→SYNCRIP) 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_INTESTINECBY1 →+0.683+3.160<.001.00631
LARGE_INTESTINEIFT27 →+0.852+3.299.003.00431
LARGE_INTESTINEINTS10 →+0.641+3.212.006.00631
LARGE_INTESTINEMED26 →+0.359+3.212.001.00631
LARGE_INTESTINEHIPK3 →+0.573+3.212.004.00631
LARGE_INTESTINERIC8B →+0.497+3.212.007.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 222 associations by consensus.

CBY1 by SYNCRIP expression — LARGE_INTESTINE

Box plot of CBY1 in SYNCRIP-low vs SYNCRIP-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration