VPS13C

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

Across TCGA cell cohorts, VPS13C mutation is significantly associated with the RNA expression of many other genes, with 434 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible VPS13C-associated genes across cancer lineages are MEP1A, GYPB, and OR52B2. Each is linked with VPS13C in more than 1 cancer types. Because this analysis shows association rather than direction, both VPS13C-to-partner and partner-to-VPS13C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MEP1A grouped by VPS13C-low versus VPS13C-high in BLOOD_Myeloma.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (VPS13C→partner) and Y-score (partner→VPS13C) 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
BLOOD_MyelomaMEP1A →+0.007+4.285<.001.00332
KIDNEYGYPB →+0.114+3.369<.001.00332
LIVEROR52B2 →+0.022+3.662.002.00532
LARGE_INTESTINERPF1 →+0.458+1.572.004.00132
LARGE_INTESTINEPPP3CC →+0.586+3.546.001<.00132
LARGE_INTESTINEZUP1 →+0.430+1.290.008.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 434 associations by consensus.

MEP1A by VPS13C expression — BLOOD_Myeloma

Box plot of MEP1A in VPS13C-low vs VPS13C-high samples in BLOOD_Myeloma.

Explore this box plot interactively →

Exploration