HNRNPLP1

RNA expression — cross-omics
Cross-omicsRNA → FUNCTION-RNAPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, HNRNPLP1 RNA expression is significantly associated with the go_rna of many other GO terms, with 6,726 significant associations in total. STAD shows the largest number of these associations.

The most reproducible HNRNPLP1-associated GO terms across cancer lineages are Peptidyl-lysine modification, Regulation of protein ubiquitination, and Regulation of post-translational protein modification. Each is linked with HNRNPLP1 in more than 21 cancer types. Because this analysis shows association rather than direction, both HNRNPLP1-to-partner and partner-to-HNRNPLP1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Peptidyl-lysine modification grouped by HNRNPLP1-low versus HNRNPLP1-high in STAD.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (HNRNPLP1→partner) and Y-score (partner→HNRNPLP1) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner GO termX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
STADPeptidyl-lysine modification →+0.043+0.176<.001<.001322
STADRegulation of protein ubiquitination →+0.052+0.227<.001<.001322
STADRegulation of post-translational protein modification →+0.050+0.176<.001<.001322
STADRegulation of microtubule cytoskeleton organization →+0.044+0.199<.001<.001322
STADRegulation of proteasomal ubiquitin-dependent protein catabolic process →+0.046+0.188<.001<.001321
TGCTNegative regulation of proteasomal ubiquitin-dependent protein catabolic process →+0.050+0.121<.001<.001321
Each partner links to its Q-omics profile. Showing the 6 strongest of 6,726 associations by consensus.

Peptidyl-lysine modification by HNRNPLP1 expression — STAD

Box plot of Peptidyl-lysine modification in HNRNPLP1-low vs HNRNPLP1-high samples in STAD.

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Exploration