RNA, U6 small nuclear 988, pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU6-988P profile across patient tissues and cancer cell-line models. RNU6-988P expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in MESO. Among the 18 cancer types available for tumor–normal comparison, RNU6-988P is differentially expressed in 3, with the highest sampling consensus in KIRP. Additionally, RNU6-988P RNA expression shows 6,530 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight MESO, KIRP, and STAD as cancer lineages where RNU6-988P 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 RNU6-988P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU6-988P survival associations across molecular data types. RNU6-988P RNA expression shows survival associations in the most cancer types (12). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU6-988P RNA expression–survival associations across cancer types. High RNU6-988P expression shows unfavorable associations in MESO, LIHC, SKCM and KIRC, but favorable associations in BLCA and CESC. 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 RNU6-988P RNA expression.
This table summarizes RNU6-988P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 3. The strongest signals are observed in KIRP for RNA.
This table ranks reproducible tumor–normal expression differences for RNU6-988P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU6-988P shows lower tumor expression in KIRP and KICH and higher tumor expression in UCEC. The KIRP box plot shows higher RNU6-988P RNA expression in normal versus tumor tissue (log2 FC = −0.175, t-test p = .025).
This table shows molecular features associated with RNU6-988P in patient tissues and cancer cell lines. In patient samples, RNU6-988P shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
