Q-omics provides the consensus-scored RPL21P30 profile across patient tissues and cancer cell-line models. RPL21P30 expression is associated with patient survival in 25 of 34 cancer types, with the highest sampling consensus in OV. Among the 18 cancer types available for tumor–normal comparison, RPL21P30 is differentially expressed in 5, with the highest sampling consensus in KICH. Additionally, RPL21P30 RNA expression shows 12,274 significant gene co-expression associations, with the highest sampling consensus in LAML. Together, these results highlight OV, KICH, and LAML as cancer lineages where RPL21P30 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 RPL21P30 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPL21P30 survival associations across molecular data types. RPL21P30 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 RPL21P30 RNA expression–survival associations across cancer types. High RPL21P30 expression shows unfavorable associations in OV, KICH and DLBC, but favorable associations in UCS, BRCA and HNSC. The OV Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .010). Together, the overview and detailed table identify OV as the clearest survival context for RPL21P30 RNA expression.
This table summarizes RPL21P30 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 KICH for RNA.
This table ranks reproducible tumor–normal expression differences for RPL21P30. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPL21P30 shows lower tumor expression in KICH, UCEC and THCA and higher tumor expression in PAAD and KIRC. The KICH box plot shows higher RPL21P30 RNA expression in normal versus tumor tissue (log2 FC = −0.083, t-test p = .015).
This table shows molecular features associated with RPL21P30 in patient tissues and cancer cell lines. In patient samples, RPL21P30 shows the broadest associations at the RNA and protein expression levels, with LAML recurring as the lineage with the largest associated feature set.
