RNF217

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

Across TCGA patient cohorts, RNF217 mutation is significantly associated with the RNA expression of many other genes, with 2,220 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RNF217-associated genes across cancer lineages are ANKRD26P2, GLA, and ENO2. Each is linked with RNF217 in more than 1 cancer types. Because this analysis shows association rather than direction, both RNF217-to-partner and partner-to-RNF217 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ANKRD26P2 grouped by RNF217-low versus RNF217-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RNF217→partner) and Y-score (partner→RNF217) 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
CESCANKRD26P2 →+0.084+5.418<.001.00532
SKCMGLA →+0.442+2.826.008.00132
SKCMENO2 →+1.173+3.472.002.00232
UCECELK1 →+0.458+2.343.004.00332
SKCMABHD8 →+0.613+3.237.001.00932
SKCMPIN1 →+0.417+3.510.003.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,220 associations by consensus.

ANKRD26P2 by RNF217 expression — CESC

Box plot of ANKRD26P2 in RNF217-low vs RNF217-high samples in CESC.

Explore this box plot interactively →

Exploration