NPHS2

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

Across TCGA patient cohorts, NPHS2 mutation is significantly associated with the RNA expression of many other genes, with 1,370 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NPHS2-associated genes across cancer lineages are MMEL1, TMEM109, and SLC3A2. Each is linked with NPHS2 in more than 2 cancer types. Because this analysis shows association rather than direction, both NPHS2-to-partner and partner-to-NPHS2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MMEL1 grouped by NPHS2-low versus NPHS2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NPHS2→partner) and Y-score (partner→NPHS2) 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
UCECMMEL1 →-0.865-3.896<.001<.00133
LUSCTMEM109 →+0.444+3.530.005.00232
LUSCSLC3A2 →+0.776+3.506.001.00232
LUSCMMP17 →+0.675+3.471.008.00232
LUSCCOL15A1 →+1.235+3.471.001.00232
LUSCRNU6-458P →+0.128+3.993<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,370 associations by consensus.

MMEL1 by NPHS2 expression — UCEC

Box plot of MMEL1 in NPHS2-low vs NPHS2-high samples in UCEC.

Explore this box plot interactively →

Exploration