NPHS1

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

Across TCGA patient cohorts, NPHS1 mutation is significantly associated with the total protein of many other genes, with 68 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NPHS1-associated genes across cancer lineages are eEF2, Rictor_pT1135, and EGFR_pY1068. Each is linked with NPHS1 in more than 3 cancer types. Because this analysis shows association rather than direction, both NPHS1-to-partner and partner-to-NPHS1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, eEF2 grouped by NPHS1-low versus NPHS1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NPHS1→partner) and Y-score (partner→NPHS1) 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
SKCMeEF2 →+0.214+2.132.039.00834
UCECRictor_pT1135 →-0.072-1.050.010.02334
LUSCEGFR_pY1068 →-0.334-1.575.035.03533
LUAD4E-BP1 →+0.568+3.012<.001.01824
UCECPCNA →+0.207+1.722<.001<.00133
UCECTFRC →+0.460+2.070.001.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 68 associations by consensus.

eEF2 by NPHS1 expression — SKCM

Box plot of eEF2 in NPHS1-low vs NPHS1-high samples in SKCM.

Explore this box plot interactively →

Exploration