ribosomal protein L12 pseudogene 49Genealiases: []
Q-omics provides the consensus-scored RPL12P49 profile across patient tissues and cancer cell-line models. RPL12P49 expression is associated with patient survival in 16 of 34 cancer types, with the highest sampling consensus in TGCT. Among the 18 cancer types available for tumor–normal comparison, RPL12P49 is differentially expressed in 1, with the highest sampling consensus in READ. Additionally, RPL12P49 RNA expression shows 6,218 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight TGCT, READ, and STAD as cancer lineages where RPL12P49 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 RPL12P49 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPL12P49 survival associations across molecular data types. RPL12P49 RNA expression shows survival associations in the most cancer types (16). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RPL12P49 RNA expression–survival associations across cancer types. High RPL12P49 expression shows unfavorable associations in TGCT, THCA, UCEC, DLBC, ACC and LIHC. The TGCT Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .002). Together, the overview and detailed table identify TGCT as the clearest survival context for RPL12P49 RNA expression.
This table summarizes RPL12P49 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 1. The strongest signals are observed in READ for RNA.
This table ranks reproducible tumor–normal expression differences for RPL12P49. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPL12P49 shows higher tumor expression in READ. The READ box plot shows higher RPL12P49 RNA expression in tumor versus normal tissue (log2 FC = +0.568, t-test p = .047).
This table shows molecular features associated with RPL12P49 in patient tissues and cancer cell lines. In patient samples, RPL12P49 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
