CSTF2T

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

Across TCGA patient cohorts, CSTF2T mutation is significantly associated with the RNA expression of many other genes, with 3,999 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CSTF2T-associated genes across cancer lineages are TSPY18P, RNU6-4P, and CEND1P1. Each is linked with CSTF2T in more than 2 cancer types. Because this analysis shows association rather than direction, both CSTF2T-to-partner and partner-to-CSTF2T results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TSPY18P grouped by CSTF2T-low versus CSTF2T-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CSTF2T→partner) and Y-score (partner→CSTF2T) 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
BRCATSPY18P →+0.072+7.473<.001.00733
UCECRNU6-4P →+0.368+1.649.001.00133
STADCEND1P1 →+0.139+4.782.001.00332
LIHCNUS1P4 →+0.066+5.758<.001.00332
LIHCTNR-IT1 →+0.078+6.902<.001<.00132
BRCARNA5SP109 →+0.477+5.505<.001.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,999 associations by consensus.

TSPY18P by CSTF2T expression — BRCA

Box plot of TSPY18P in CSTF2T-low vs CSTF2T-high samples in BRCA.

Explore this box plot interactively →

Exploration