RANBP3L

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

Across TCGA patient cohorts, RANBP3L mutation is significantly associated with the RNA expression of many other genes, with 442 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RANBP3L-associated genes across cancer lineages are SNHG10, SMIM4, and TMEM126A. Each is linked with RANBP3L in more than 1 cancer types. Because this analysis shows association rather than direction, both RANBP3L-to-partner and partner-to-RANBP3L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNHG10 grouped by RANBP3L-low versus RANBP3L-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RANBP3L→partner) and Y-score (partner→RANBP3L) 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
SKCMSNHG10 →+0.646+3.341.001.00532
UCECSMIM4 →+0.412+2.457.008.00132
UCECTMEM126A →+0.404+2.513.002.00932
UCECSNAPC5 →+0.343+3.375.004.00432
LUADRN7SKP177 →+0.119+4.984<.001.00532
UCECCAPZB →+0.298+3.512.007.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 442 associations by consensus.

SNHG10 by RANBP3L expression — SKCM

Box plot of SNHG10 in RANBP3L-low vs RANBP3L-high samples in SKCM.

Explore this box plot interactively →

Exploration