SYNGR2

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

Across TCGA patient cohorts, SYNGR2 mutation is significantly associated with the RNA expression of many other genes, with 248 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SYNGR2-associated genes across cancer lineages are RNU6-1318P, OR11H12, and DUX4L47. Each is linked with SYNGR2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SYNGR2-to-partner and partner-to-SYNGR2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-1318P grouped by SYNGR2-low versus SYNGR2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SYNGR2→partner) and Y-score (partner→SYNGR2) 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
UCECRNU6-1318P →+0.426+3.358<.001.00132
SKCMOR11H12 →+0.077+6.199<.001.00131
SKCMDUX4L47 →+0.133+5.867<.001.00331
SKCMRN7SL498P →+0.168+5.097<.001.00831
BLCAGUCA1C →+0.283+3.193.002.00631
BLCATSPY2 →+0.672+3.435<.001.00731
Each partner links to its Q-omics profile. Showing the 6 strongest of 248 associations by consensus.

RNU6-1318P by SYNGR2 expression — UCEC

Box plot of RNU6-1318P in SYNGR2-low vs SYNGR2-high samples in UCEC.

Explore this box plot interactively →

Exploration