HCG4B

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

Across TCGA patient cohorts, HCG4B mutation is significantly associated with the RNA expression of many other genes, with 24 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HCG4B-associated genes across cancer lineages are SALL4P2, SELENOTP2, and RNA5SP414. Each is linked with HCG4B in more than 1 cancer types. Because this analysis shows association rather than direction, both HCG4B-to-partner and partner-to-HCG4B 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 (HCG4B→partner) and Y-score (partner→HCG4B) 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
SKCMSALL4P2 →+0.032+5.436<.001.00531
UCECSELENOTP2 →+0.280+4.233<.001.00931
UCECRNA5SP414 →+1.391+4.840<.001.00331
SKCMRNU6-234P →+0.498+5.771<.001.00331
UCECMIR4797 →+1.117+4.633<.001.00431
UCECRNU6-1082P →+0.506+4.551<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 24 associations by consensus.

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