NINL

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

Across TCGA patient cohorts, NINL mutation is significantly associated with the RNA expression of many other genes, with 3,619 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NINL-associated genes across cancer lineages are NSD2, NUSAP1, and WDR76. Each is linked with NINL in more than 4 cancer types. Because this analysis shows association rather than direction, both NINL-to-partner and partner-to-NINL results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NSD2 grouped by NINL-low versus NINL-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NINL→partner) and Y-score (partner→NINL) 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
UCECNSD2 →+0.396+1.103.001.00935
UCECNUSAP1 →+0.553+2.091<.001<.00135
UCECWDR76 →+0.583+1.565<.001<.00134
STADEIF5A →+0.842+3.618<.001.00134
UCECSGTA →+0.443+2.099<.001<.00134
UCECTBC1D13 →+0.323+2.102<.001<.00134
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,619 associations by consensus.

NSD2 by NINL expression — UCEC

Box plot of NSD2 in NINL-low vs NINL-high samples in UCEC.

Explore this box plot interactively →

Exploration