EIF2S1

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

Across TCGA patient cohorts, EIF2S1 mutation is significantly associated with the RNA expression of many other genes, with 2,083 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible EIF2S1-associated genes across cancer lineages are RNA5SP131, NPLP1, and RN7SL248P. Each is linked with EIF2S1 in more than 1 cancer types. Because this analysis shows association rather than direction, both EIF2S1-to-partner and partner-to-EIF2S1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNA5SP131 grouped by EIF2S1-low versus EIF2S1-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (EIF2S1→partner) and Y-score (partner→EIF2S1) 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
BLCARNA5SP131 →+0.263+5.722<.001.00132
COADNPLP1 →+0.257+5.080<.001.00832
UCECRN7SL248P →+0.067+3.400<.001.00332
UCECRNU6-628P →+0.464+2.236<.001.00232
CESCNEUROD6 →+0.015+4.812.002.00631
CESCLINC00314 →+0.045+4.669<.001.00731
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,083 associations by consensus.

RNA5SP131 by EIF2S1 expression — BLCA

Box plot of RNA5SP131 in EIF2S1-low vs EIF2S1-high samples in BLCA.

Explore this box plot interactively →

Exploration