RNA, U6 small nuclear 969, pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU6-969P profile across patient tissues and cancer cell-line models. RNU6-969P expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in BLCA. Among the 18 cancer types available for tumor–normal comparison, RNU6-969P is differentially expressed in 5, with the highest sampling consensus in KIRP. Additionally, RNU6-969P RNA expression shows 7,179 significant protein co-abundance associations, with the highest sampling consensus in HNSC. Together, these results highlight BLCA, KIRP, and HNSC as cancer lineages where RNU6-969P 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 RNU6-969P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU6-969P survival associations across molecular data types. RNU6-969P RNA expression shows survival associations in the most cancer types (19). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU6-969P RNA expression–survival associations across cancer types. High RNU6-969P expression shows unfavorable associations in MESO, THCA, KIRP, CESC and LUSC, but favorable associations in BLCA. The BLCA Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .002). Together, the overview and detailed table identify BLCA as the clearest survival context for RNU6-969P RNA expression.
This table summarizes RNU6-969P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in KIRP for RNA.
This table ranks reproducible tumor–normal expression differences for RNU6-969P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU6-969P shows lower tumor expression in KIRP and COAD and higher tumor expression in HNSC, CHOL and READ. The KIRP box plot shows higher RNU6-969P RNA expression in normal versus tumor tissue (log2 FC = −0.245, t-test p = .010).
This table shows molecular features associated with RNU6-969P in patient tissues and cancer cell lines. In patient samples, RNU6-969P shows the broadest associations at the RNA and protein expression levels, with HNSC recurring as the lineage with the largest associated feature set.
