RNA, U6 small nuclear 212, pseudogeneGenealiases: []
Q-omics provides the consensus-scored RNU6-212P profile across patient tissues and cancer cell-line models. RNU6-212P expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in UCEC. Among the 18 cancer types available for tumor–normal comparison, RNU6-212P is differentially expressed in 2, with the highest sampling consensus in THCA. Additionally, RNU6-212P RNA expression shows 6,541 significant protein co-abundance associations, with the highest sampling consensus in CCRCC. Together, these results highlight UCEC, THCA, and CCRCC as cancer lineages where RNU6-212P 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 RNU6-212P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNU6-212P survival associations across molecular data types. RNU6-212P RNA expression shows survival associations in the most cancer types (12). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNU6-212P RNA expression–survival associations across cancer types. High RNU6-212P expression shows unfavorable associations in UCEC, ACC, SKCM, HNSC and LIHC, but favorable associations in STAD. The UCEC 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 UCEC as the clearest survival context for RNU6-212P RNA expression.
This table summarizes RNU6-212P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in THCA for RNA.
This table ranks reproducible tumor–normal expression differences for RNU6-212P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNU6-212P shows lower tumor expression in THCA and higher tumor expression in STAD. The THCA box plot shows higher RNU6-212P RNA expression in normal versus tumor tissue (log2 FC = −0.213, t-test p < 0.001).
This table shows molecular features associated with RNU6-212P in patient tissues and cancer cell lines. In patient samples, RNU6-212P shows the broadest associations at the RNA and protein expression levels, with CCRCC recurring as the lineage with the largest associated feature set.
