RNA, U2 small nuclear 63, pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU2-63P profile across patient tissues and cancer cell-line models. RNU2-63P expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, RNU2-63P is differentially expressed in 6, with the highest sampling consensus in THCA. Additionally, RNU2-63P RNA expression shows 8,947 significant protein co-abundance associations, with the highest sampling consensus in CCRCC. Together, these results highlight KIRC, THCA, and CCRCC as cancer lineages where RNU2-63P 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 RNU2-63P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU2-63P survival associations across molecular data types. RNU2-63P RNA expression shows survival associations in the most cancer types (17). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU2-63P RNA expression–survival associations across cancer types. High RNU2-63P expression shows unfavorable associations in KIRC, THYM, CHOL and COAD, but favorable associations in PAAD and READ. The KIRC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .001). Together, the overview and detailed table identify KIRC as the clearest survival context for RNU2-63P RNA expression.
This table summarizes RNU2-63P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 6. The strongest signals are observed in THCA for RNA.
This table ranks reproducible tumor–normal expression differences for RNU2-63P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU2-63P shows lower tumor expression in THCA and KICH and higher tumor expression in UCEC, STAD, LUAD and LIHC. The THCA box plot shows higher RNU2-63P RNA expression in normal versus tumor tissue (log2 FC = −1.505, t-test p < 0.001).
This table shows molecular features associated with RNU2-63P in patient tissues and cancer cell lines. In patient samples, RNU2-63P shows the broadest associations at the RNA and protein expression levels, with CCRCC recurring as the lineage with the largest associated feature set.
