SNRK

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

Across TCGA patient cohorts, SNRK mutation is significantly associated with the RNA expression of many other genes, with 4,899 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNRK-associated genes across cancer lineages are RN7SL134P, NF1P10, and RN7SL248P. Each is linked with SNRK in more than 3 cancer types. Because this analysis shows association rather than direction, both SNRK-to-partner and partner-to-SNRK results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL134P grouped by SNRK-low versus SNRK-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNRK→partner) and Y-score (partner→SNRK) 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
UCECRN7SL134P →+0.075+1.645.003.00534
CESCNF1P10 →+0.390+7.154<.001<.00133
SKCMRN7SL248P →+0.030+4.025<.001.00733
SKCMRNU6-718P →+0.306+2.502.002.00532
UCECMIR6803 →+0.100+3.893<.001<.00132
UCECLIN7C →+0.532+2.214<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,899 associations by consensus.

RN7SL134P by SNRK expression — UCEC

Box plot of RN7SL134P in SNRK-low vs SNRK-high samples in UCEC.

Explore this box plot interactively →

Exploration