RNA, U7 small nuclear 193 pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU7-193P profile across patient tissues and cancer cell-line models. RNU7-193P expression is associated with patient survival in 10 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, RNU7-193P is differentially expressed in 1, with the highest sampling consensus in HNSC. Additionally, RNU7-193P RNA expression shows 6,344 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight KIRC, HNSC, and STAD as cancer lineages where RNU7-193P 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 RNU7-193P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU7-193P survival associations across molecular data types. RNU7-193P RNA expression shows survival associations in the most cancer types (10). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU7-193P RNA expression–survival associations across cancer types. High RNU7-193P expression shows unfavorable associations in KIRC, KICH, ACC, READ and KIRP, but favorable associations in PAAD. 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 RNU7-193P RNA expression.
This table summarizes RNU7-193P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 1. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for RNU7-193P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU7-193P shows higher tumor expression in HNSC. The HNSC box plot shows higher RNU7-193P RNA expression in tumor versus normal tissue (log2 FC = +0.277, t-test p = .036).
This table shows molecular features associated with RNU7-193P in patient tissues and cancer cell lines. In patient samples, RNU7-193P shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
