RNA, U7 small nuclear 18 pseudogeneGenealiases: RNU7-142P · U7.18
Q-omics provides the consensus-scored RNU7-18P profile across patient tissues and cancer cell-line models. RNU7-18P expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, RNU7-18P is differentially expressed in 6, with the highest sampling consensus in HNSC. Additionally, RNU7-18P RNA expression shows 8,482 significant protein co-abundance associations, with the highest sampling consensus in CCRCC. Together, these results highlight UVM, HNSC, and CCRCC as cancer lineages where RNU7-18P 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 RNU7-18P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU7-18P survival associations across molecular data types. RNU7-18P RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU7-18P RNA expression–survival associations across cancer types. High RNU7-18P expression shows unfavorable associations in UVM, THCA, GBM, KICH, LGG and KIRC. The UVM 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 UVM as the clearest survival context for RNU7-18P RNA expression.
This table summarizes RNU7-18P 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 HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for RNU7-18P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU7-18P shows lower tumor expression in PAAD and higher tumor expression in HNSC, BLCA, BRCA, STAD and COAD. The HNSC box plot shows higher RNU7-18P RNA expression in tumor versus normal tissue (log2 FC = +0.459, t-test p < 0.001).
This table shows molecular features associated with RNU7-18P in patient tissues and cancer cell lines. In patient samples, RNU7-18P shows the broadest associations at the RNA and protein expression levels, with CCRCC recurring as the lineage with the largest associated feature set.
