Q-omics provides the consensus-scored MIR648 profile across patient tissues and cancer cell-line models. MIR648 expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, MIR648 is differentially expressed in 3, with the highest sampling consensus in BRCA. Additionally, MIR648 RNA expression shows 8,977 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight KICH, BRCA, and GBM as cancer lineages where MIR648 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 MIR648 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MIR648 survival associations across molecular data types. MIR648 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 MIR648 RNA expression–survival associations across cancer types. High MIR648 expression shows unfavorable associations in KICH, DLBC, UCEC, MESO and LUSC, but favorable associations in CESC. 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 MIR648 RNA expression.
This table summarizes MIR648 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 3. The strongest signals are observed in BRCA for RNA.
This table ranks reproducible tumor–normal expression differences for MIR648. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR648 shows lower tumor expression in BRCA, KIRP and KIRC. The BRCA box plot shows higher MIR648 RNA expression in normal versus tumor tissue (log2 FC = −0.161, t-test p = .020).
This table shows molecular features associated with MIR648 in patient tissues and cancer cell lines. In patient samples, MIR648 shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set.
