Q-omics provides the consensus-scored RPL13P12 profile across patient tissues and cancer cell-line models. RPL13P12 expression is associated with patient survival in 25 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, RPL13P12 is differentially expressed in 6, with the highest sampling consensus in COAD. Additionally, RPL13P12 RNA expression shows 14,598 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight ACC, COAD, and THYM as cancer lineages where RPL13P12 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 RPL13P12 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPL13P12 survival associations across molecular data types. RPL13P12 RNA expression shows survival associations in the most cancer types (25). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RPL13P12 RNA expression–survival associations across cancer types. High RPL13P12 expression shows unfavorable associations in ACC, LUAD and PRAD, but favorable associations in BRCA, CESC and KIRC. The ACC 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 ACC as the clearest survival context for RPL13P12 RNA expression.
This table summarizes RPL13P12 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 RPL13P12. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPL13P12 shows lower tumor expression in BRCA and higher tumor expression in COAD, KIRC, KIRP, CHOL and LIHC. The COAD box plot shows higher RPL13P12 RNA expression in tumor versus normal tissue (log2 FC = +2.401, t-test p < 0.001).
This table shows molecular features associated with RPL13P12 in patient tissues and cancer cell lines. In patient samples, RPL13P12 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
