SRSF9

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

Across TCGA patient cohorts, SRSF9 mutation is significantly associated with the RNA expression of many other genes, with 49 significant associations in total. CESC shows the largest number of these associations.

The most reproducible SRSF9-associated genes across cancer lineages are RNU2-47P, COPRSP1, and RNU4ATAC11P. Each is linked with SRSF9 in more than 1 cancer types. Because this analysis shows association rather than direction, both SRSF9-to-partner and partner-to-SRSF9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU2-47P grouped by SRSF9-low versus SRSF9-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SRSF9→partner) and Y-score (partner→SRSF9) 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
BRCARNU2-47P →+0.628+8.055<.001.00732
CESCCOPRSP1 →+0.085+4.653<.001.00431
CESCRNU4ATAC11P →+0.292+4.705.003.00331
CESCRNU6-1110P →+0.881+4.760<.001.00331
CESCLINC01414 →+0.164+4.320.003.00731
CESCOR7E10P →+0.040+5.144<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 49 associations by consensus.

RNU2-47P by SRSF9 expression — BRCA

Box plot of RNU2-47P in SRSF9-low vs SRSF9-high samples in BRCA.

Explore this box plot interactively →

Exploration