HNF1A

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

Across TCGA patient cohorts, HNF1A mutation is significantly associated with the RNA expression of many other genes, with 1,490 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HNF1A-associated genes across cancer lineages are RNU2-24P, MIR6893, and CERS3-AS1. Each is linked with HNF1A in more than 2 cancer types. Because this analysis shows association rather than direction, both HNF1A-to-partner and partner-to-HNF1A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU2-24P grouped by HNF1A-low versus HNF1A-high in LIHC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (HNF1A→partner) and Y-score (partner→HNF1A) 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
LIHCRNU2-24P →+0.210+3.866.005.00233
COADMIR6893 →+0.582+3.096<.001.00533
LIHCCERS3-AS1 →+0.478+3.630.007.00832
SARCKRTAP19-7 →+0.085+5.977<.001.00132
SARCLINC01438 →+0.162+5.152<.001.00332
SARCMIR6821 →+0.550+4.291.002.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,490 associations by consensus.

RNU2-24P by HNF1A expression — LIHC

Box plot of RNU2-24P in HNF1A-low vs HNF1A-high samples in LIHC.

Explore this box plot interactively →

Exploration