ARHGEF33

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

Across TCGA patient cohorts, ARHGEF33 mutation is significantly associated with the RNA expression of many other genes, with 1,989 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible ARHGEF33-associated genes across cancer lineages are RN7SL713P, SUMO2P12, and RN7SL810P. Each is linked with ARHGEF33 in more than 1 cancer types. Because this analysis shows association rather than direction, both ARHGEF33-to-partner and partner-to-ARHGEF33 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ARHGEF33→partner) and Y-score (partner→ARHGEF33) 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
BRCARN7SL713P →+0.435+5.231<.001.00132
READSUMO2P12 →+0.871+5.039<.001.00832
READRN7SL810P →+0.382+6.257<.001.00132
READTCF4-AS1 →+0.231+6.257<.001.00132
BRCARN7SL361P →+0.176+5.211<.001.00132
UCECTUBGCP5 →+0.397+2.370.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,989 associations by consensus.

Exploration