RNA, U2 small nuclear 42, pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU2-42P profile across patient tissues and cancer cell-line models. RNU2-42P expression is associated with patient survival in 7 of 34 cancer types, with the highest sampling consensus in DLBC. Among the 18 cancer types available for tumor–normal comparison, RNU2-42P is differentially expressed in 1, with the highest sampling consensus in ESCA. Additionally, RNU2-42P RNA expression shows 5,965 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight DLBC, ESCA, and STAD as cancer lineages where RNU2-42P shows reproducible signals across survival, tumor–normal expression, and patient cross-omics analyses.
Every result is evaluated using two consensus scores. Sampling consensus measures how consistently a finding is reproduced within a cancer lineage across different conditions. Lineage consensus measures how broadly the result is shared across cancer types, distinguishing pan-cancer signals from lineage-specific patterns.
Premium analyses for RNU2-42P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU2-42P survival associations across molecular data types. RNU2-42P RNA expression shows survival associations in the most cancer types (7). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU2-42P RNA expression–survival associations across cancer types. High RNU2-42P expression shows unfavorable associations in DLBC, UCEC, BLCA, LGG, THYM and MESO. The DLBC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p < 0.001). Together, the overview and detailed table identify DLBC as the clearest survival context for RNU2-42P RNA expression.
This table summarizes RNU2-42P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 1. The strongest signals are observed in ESCA for RNA.
This table ranks reproducible tumor–normal expression differences for RNU2-42P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU2-42P shows lower tumor expression in ESCA. The ESCA box plot shows higher RNU2-42P RNA expression in normal versus tumor tissue (log2 FC = −0.796, t-test p = .047).
This table shows molecular features associated with RNU2-42P in patient tissues and cancer cell lines. In patient samples, RNU2-42P shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
