Q-omics provides the consensus-scored RN7SL128P profile across patient tissues and cancer cell-line models. RN7SL128P expression is associated with patient survival in 16 of 34 cancer types, with the highest sampling consensus in MESO. Among the 18 cancer types available for tumor–normal comparison, RN7SL128P is differentially expressed in 6, with the highest sampling consensus in COAD. Additionally, RN7SL128P RNA expression shows 12,970 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight MESO, COAD, and ACC as cancer lineages where RN7SL128P 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 RN7SL128P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RN7SL128P survival associations across molecular data types. RN7SL128P RNA expression shows survival associations in the most cancer types (16). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RN7SL128P RNA expression–survival associations across cancer types. High RN7SL128P expression shows unfavorable associations in MESO, KICH, THCA and LGG, but favorable associations in LAML and BRCA. The MESO Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .003). Together, the overview and detailed table identify MESO as the clearest survival context for RN7SL128P RNA expression.
This table summarizes RN7SL128P 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 COAD for RNA.
This table ranks reproducible tumor–normal expression differences for RN7SL128P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RN7SL128P shows lower tumor expression in STAD, LUAD and THCA and higher tumor expression in COAD, BRCA and KIRP. The COAD box plot shows higher RN7SL128P RNA expression in tumor versus normal tissue (log2 FC = +0.411, t-test p = .011).
This table shows molecular features associated with RN7SL128P in patient tissues and cancer cell lines. In patient samples, RN7SL128P shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
