CDKN1A

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

Across TCGA patient cohorts, CDKN1A mutation is significantly associated with the RNA expression of many other genes, with 338 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CDKN1A-associated genes across cancer lineages are HMGB1P22, RNU6-1118P, and RN7SL776P. Each is linked with CDKN1A in more than 1 cancer types. Because this analysis shows association rather than direction, both CDKN1A-to-partner and partner-to-CDKN1A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, HMGB1P22 grouped by CDKN1A-low versus CDKN1A-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CDKN1A→partner) and Y-score (partner→CDKN1A) 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
CESCHMGB1P22 →+0.287+4.539<.001.00832
BLCARNU6-1118P →+0.191+4.040<.001.00732
BLCARN7SL776P →+0.045+5.051<.001.00132
SKCMRN7SL111P →+0.171+4.310.004.00332
UCECRNU6-894P →+0.261+3.879<.001.00932
UCECGUSBP16 →+0.080+2.600<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 338 associations by consensus.

HMGB1P22 by CDKN1A expression — CESC

Box plot of HMGB1P22 in CDKN1A-low vs CDKN1A-high samples in CESC.

Explore this box plot interactively →

Exploration