SEPHS2

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

Across TCGA cell cohorts, SEPHS2 mutation is significantly associated with the RNA expression of many other genes, with 13 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible SEPHS2-associated genes across cancer lineages are GFRA4, CALHM4, and OR10K2. Each is linked with SEPHS2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SEPHS2-to-partner and partner-to-SEPHS2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, GFRA4 grouped by SEPHS2-low versus SEPHS2-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SEPHS2→partner) and Y-score (partner→SEPHS2) 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
BLOOD_LeukemiaGFRA4 →+0.308+4.409<.001.00531
BLOOD_LeukemiaCALHM4 →+0.038+5.269<.001<.00131
BLOOD_LeukemiaOR10K2 →+0.060+4.705<.001.00331
BLOOD_LeukemiaOR10T2 →+0.889+4.276<.001.00731
BLOOD_LeukemiaOR10R2 →+1.909+4.551<.001.00431
BLOOD_LeukemiaTSSK1B →+0.014+4.874<.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 13 associations by consensus.

GFRA4 by SEPHS2 expression — BLOOD_Leukemia

Box plot of GFRA4 in SEPHS2-low vs SEPHS2-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration