RCC2

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

Across TCGA patient cohorts, RCC2 mutation is significantly associated with the RNA expression of many other genes, with 1,899 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RCC2-associated genes across cancer lineages are MIR6782, RN7SKP60, and VN1R93P. Each is linked with RCC2 in more than 1 cancer types. Because this analysis shows association rather than direction, both RCC2-to-partner and partner-to-RCC2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR6782 grouped by RCC2-low versus RCC2-high in KIRC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RCC2→partner) and Y-score (partner→RCC2) 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
KIRCMIR6782 →+0.554+5.316<.001.00632
SKCMRN7SKP60 →+0.119+4.469<.001.00632
LIHCVN1R93P →+0.060+5.149.002.00332
LIHCRNU6-973P →+0.242+4.647<.001.00732
LIHCLINC01047 →+0.052+6.343<.001<.00132
LIHCRN7SL861P →+0.154+5.547<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,899 associations by consensus.

MIR6782 by RCC2 expression — KIRC

Box plot of MIR6782 in RCC2-low vs RCC2-high samples in KIRC.

Explore this box plot interactively →

Exploration