RNA, U6 small nuclear 762, pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU6-762P profile across patient tissues and cancer cell-line models. RNU6-762P expression is associated with patient survival in 23 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, RNU6-762P is differentially expressed in 14, with the highest sampling consensus in BLCA. Additionally, RNU6-762P RNA expression shows 17,195 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight KIRC, BLCA, and UVM as cancer lineages where RNU6-762P 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 RNU6-762P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU6-762P survival associations across molecular data types. RNU6-762P RNA expression shows survival associations in the most cancer types (23). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU6-762P RNA expression–survival associations across cancer types. High RNU6-762P expression shows unfavorable associations in KIRC, ACC, LIHC, THCA and LGG, but favorable associations in BLCA. The KIRC 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 KIRC as the clearest survival context for RNU6-762P RNA expression.
This table summarizes RNU6-762P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 14. The strongest signals are observed in LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for RNU6-762P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU6-762P shows higher tumor expression in BLCA, COAD, LUSC, LIHC, KIRC and UCEC. The BLCA box plot shows higher RNU6-762P RNA expression in tumor versus normal tissue (log2 FC = +1.251, t-test p = .003).
This table shows molecular features associated with RNU6-762P in patient tissues and cancer cell lines. In patient samples, RNU6-762P shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
