Q-omics provides the consensus-scored MIR647 profile across patient tissues and cancer cell-line models. MIR647 expression is associated with patient survival in 26 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, MIR647 is differentially expressed in 13, with the highest sampling consensus in COAD. Additionally, MIR647 RNA expression shows 18,987 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight KIRC, COAD, and UVM as cancer lineages where MIR647 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 MIR647 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MIR647 survival associations across molecular data types. MIR647 RNA expression shows survival associations in the most cancer types (26). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible MIR647 RNA expression–survival associations across cancer types. High MIR647 expression shows unfavorable associations in KIRC, PRAD and THCA, but favorable associations in UCS, BLCA and PAAD. The KIRC 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 KIRC as the clearest survival context for MIR647 RNA expression.
This table summarizes MIR647 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 13. The strongest signals are observed in BLCA for RNA.
This table ranks reproducible tumor–normal expression differences for MIR647. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR647 shows higher tumor expression in COAD, BLCA, KICH, KIRC, LIHC and STAD. The COAD box plot shows higher MIR647 RNA expression in tumor versus normal tissue (log2 FC = +1.990, t-test p < 0.001).
This table shows molecular features associated with MIR647 in patient tissues and cancer cell lines. In patient samples, MIR647 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
