HNRNPA1P12

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

Across TCGA patient cohorts, HNRNPA1P12 mutation is significantly associated with the RNA expression of many other genes, with 106 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HNRNPA1P12-associated genes across cancer lineages are PHBP6, FTH1P9, and LINC00604. Each is linked with HNRNPA1P12 in more than 1 cancer types. Because this analysis shows association rather than direction, both HNRNPA1P12-to-partner and partner-to-HNRNPA1P12 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 (HNRNPA1P12→partner) and Y-score (partner→HNRNPA1P12) 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
LUADPHBP6 →+0.077+5.444<.001.00232
LUSCFTH1P9 →+0.128+4.993.002.00332
SKCMLINC00604 →+0.141+3.351<.001.00831
SKCMASS1P8 →+0.035+4.302<.001.00731
SKCMTET2-AS1 →+0.397+3.885<.001.00231
SKCMLINC00838 →+0.025+3.300<.001.00431
Each partner links to its Q-omics profile. Showing the 6 strongest of 106 associations by consensus.

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