RNA, U1 small nuclear 133, pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU1-133P profile across patient tissues and cancer cell-line models. RNU1-133P expression is associated with patient survival in 9 of 34 cancer types, with the highest sampling consensus in MESO. Among the 18 cancer types available for tumor–normal comparison, RNU1-133P is differentially expressed in 2, with the highest sampling consensus in BRCA. Additionally, RNU1-133P RNA expression shows 9,172 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight MESO, BRCA, and THYM as cancer lineages where RNU1-133P 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 RNU1-133P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU1-133P survival associations across molecular data types. RNU1-133P RNA expression shows survival associations in the most cancer types (9), followed by mutation status (1). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU1-133P RNA expression–survival associations across cancer types. High RNU1-133P expression shows unfavorable associations in MESO, BLCA, HNSC, STAD, KIRP and LUAD. The MESO 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 MESO as the clearest survival context for RNU1-133P RNA expression.
This table summarizes RNU1-133P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in BRCA for RNA.
This table ranks reproducible tumor–normal expression differences for RNU1-133P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU1-133P shows lower tumor expression in PRAD and higher tumor expression in BRCA. The BRCA box plot shows higher RNU1-133P RNA expression in tumor versus normal tissue (log2 FC = +0.121, t-test p = .043).
This table shows molecular features associated with RNU1-133P in patient tissues and cancer cell lines. In patient samples, RNU1-133P shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
