Q-omics provides the consensus-scored MIR4713 profile across patient tissues and cancer cell-line models. MIR4713 expression is associated with patient survival in 6 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, MIR4713 is differentially expressed in 1, with the highest sampling consensus in STAD. Additionally, MIR4713 RNA expression shows 4,896 significant gene co-expression associations, with the highest sampling consensus in UCEC. Together, these results highlight KICH, STAD, and UCEC as cancer lineages where MIR4713 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 MIR4713 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MIR4713 survival associations across molecular data types. MIR4713 RNA expression shows survival associations in the most cancer types (6). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible MIR4713 RNA expression–survival associations across cancer types. High MIR4713 expression shows unfavorable associations in KICH, BRCA, UCEC, LUSC, DLBC and LUAD. The KICH 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 KICH as the clearest survival context for MIR4713 RNA expression.
This table summarizes MIR4713 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 STAD for RNA.
This table ranks reproducible tumor–normal expression differences for MIR4713. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR4713 shows higher tumor expression in STAD. The STAD box plot shows higher MIR4713 RNA expression in tumor versus normal tissue (log2 FC = +0.130, t-test p = .049).
This table shows molecular features associated with MIR4713 in patient tissues and cancer cell lines. In patient samples, MIR4713 shows the broadest associations at the RNA and protein expression levels, with UCEC recurring as the lineage with the largest associated feature set.
