Q-omics provides the consensus-scored RN7SL272P profile across patient tissues and cancer cell-line models. RN7SL272P expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in CESC. Among the 18 cancer types available for tumor–normal comparison, RN7SL272P is differentially expressed in 4, with the highest sampling consensus in UCEC. Additionally, RN7SL272P RNA expression shows 6,512 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight CESC, UCEC, and TGCT as cancer lineages where RN7SL272P 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 RN7SL272P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RN7SL272P survival associations across molecular data types. RN7SL272P RNA expression shows survival associations in the most cancer types (17). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RN7SL272P RNA expression–survival associations across cancer types. High RN7SL272P expression shows unfavorable associations in CESC, KIRC, GBM, THCA, LUAD and PCPG. The CESC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .013). Together, the overview and detailed table identify CESC as the clearest survival context for RN7SL272P RNA expression.
This table summarizes RN7SL272P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 4. The strongest signals are observed in UCEC for RNA.
This table ranks reproducible tumor–normal expression differences for RN7SL272P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RN7SL272P shows lower tumor expression in COAD, STAD and THCA and higher tumor expression in UCEC. The UCEC box plot shows higher RN7SL272P RNA expression in tumor versus normal tissue (log2 FC = +0.455, t-test p = .033).
This table shows molecular features associated with RN7SL272P in patient tissues and cancer cell lines. In patient samples, RN7SL272P shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
