SEPHS2

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

Across TCGA patient cohorts, SEPHS2 mutation is significantly associated with the total protein of many other genes, with 18 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SEPHS2-associated genes across cancer lineages are EGFR_pY1068, ERK2, and FOXO3a_pS318_S321. 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, EGFR_pY1068 grouped by SEPHS2-low versus SEPHS2-high in UCEC.

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
UCECEGFR_pY1068 →-0.282-3.000.025.03631
UCECERK2 →+0.274+2.321.004.03531
UCECFOXO3a_pS318_S321 →-0.177-2.321.004.03531
UCECJNK_pT183_Y185 →-0.274-2.999.001.03531
UCECmTOR_pS2448 →-0.196-2.980.008.03631
UCECP-Cadherin →-0.171-2.999.018.03531
Each partner links to its Q-omics profile. Showing the 6 strongest of 18 associations by consensus.

EGFR_pY1068 by SEPHS2 expression — UCEC

Box plot of EGFR_pY1068 in SEPHS2-low vs SEPHS2-high samples in UCEC.

Explore this box plot interactively →

Exploration