Q-omics provides the consensus-scored KCNMA1-AS3 profile across patient tissues and cancer cell-line models. KCNMA1-AS3 expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in THCA. Among the 18 cancer types available for tumor–normal comparison, KCNMA1-AS3 is differentially expressed in 3, with the highest sampling consensus in KIRC. Additionally, KCNMA1-AS3 RNA expression shows 10,361 significant protein co-abundance associations, with the highest sampling consensus in BRCA. Together, these results highlight THCA, KIRC, and BRCA as cancer lineages where KCNMA1-AS3 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 KCNMA1-AS3 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes KCNMA1-AS3 survival associations across molecular data types. KCNMA1-AS3 RNA expression shows survival associations in the most cancer types (19). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible KCNMA1-AS3 RNA expression–survival associations across cancer types. High KCNMA1-AS3 expression shows unfavorable associations in THCA, UVM, BLCA, LAML and CHOL, but favorable associations in SKCM. The THCA Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .001). Together, the overview and detailed table identify THCA as the clearest survival context for KCNMA1-AS3 RNA expression.
This table summarizes KCNMA1-AS3 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 KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for KCNMA1-AS3. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. KCNMA1-AS3 shows lower tumor expression in THCA and higher tumor expression in KIRC and PRAD. The KIRC box plot shows higher KCNMA1-AS3 RNA expression in tumor versus normal tissue (log2 FC = +0.057, t-test p = .001).
This table shows molecular features associated with KCNMA1-AS3 in patient tissues and cancer cell lines. In patient samples, KCNMA1-AS3 shows the broadest associations at the RNA and protein expression levels, with BRCA recurring as the lineage with the largest associated feature set.
