Q-omics provides the consensus-scored RSL24D1P1 profile across patient tissues and cancer cell-line models. RSL24D1P1 expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in LIHC. Among the 18 cancer types available for tumor–normal comparison, RSL24D1P1 is differentially expressed in 5, with the highest sampling consensus in COAD. Additionally, RSL24D1P1 RNA expression shows 6,735 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight LIHC, COAD, and ACC as cancer lineages where RSL24D1P1 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 RSL24D1P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RSL24D1P1 survival associations across molecular data types. RSL24D1P1 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 RSL24D1P1 RNA expression–survival associations across cancer types. High RSL24D1P1 expression shows unfavorable associations in LIHC, CHOL, UVM and ESCA, but favorable associations in OV and MESO. The LIHC 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 LIHC as the clearest survival context for RSL24D1P1 RNA expression.
This table summarizes RSL24D1P1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for RSL24D1P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RSL24D1P1 shows lower tumor expression in COAD, UCEC, READ and THCA and higher tumor expression in KIRC. The COAD box plot shows higher RSL24D1P1 RNA expression in normal versus tumor tissue (log2 FC = −0.458, t-test p < 0.001).
This table shows molecular features associated with RSL24D1P1 in patient tissues and cancer cell lines. In patient samples, RSL24D1P1 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
