Q-omics provides the consensus-scored RN7SL329P profile across patient tissues and cancer cell-line models. RN7SL329P expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, RN7SL329P is differentially expressed in 4, with the highest sampling consensus in STAD. Additionally, RN7SL329P RNA expression shows 7,296 significant gene co-expression associations, with the highest sampling consensus in LAML. Together, these results highlight KICH, STAD, and LAML as cancer lineages where RN7SL329P 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 RN7SL329P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RN7SL329P survival associations across molecular data types. RN7SL329P 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 RN7SL329P RNA expression–survival associations across cancer types. High RN7SL329P expression shows unfavorable associations in KICH, LUSC, PAAD, UCS, READ and COAD. The KICH 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 KICH as the clearest survival context for RN7SL329P RNA expression.
This table summarizes RN7SL329P 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 BRCA for RNA.
This table ranks reproducible tumor–normal expression differences for RN7SL329P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RN7SL329P shows lower tumor expression in THCA and higher tumor expression in STAD, BRCA and LIHC. The STAD box plot shows higher RN7SL329P RNA expression in tumor versus normal tissue (log2 FC = +0.445, t-test p = .003).
This table shows molecular features associated with RN7SL329P in patient tissues and cancer cell lines. In patient samples, RN7SL329P shows the broadest associations at the RNA and protein expression levels, with LAML recurring as the lineage with the largest associated feature set.
