long intergenic non-protein coding RNA 2634Genealiases: []
Q-omics provides the consensus-scored LINC02634 profile across patient tissues and cancer cell-line models. LINC02634 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in BLCA. Among the 18 cancer types available for tumor–normal comparison, LINC02634 is differentially expressed in 7, with the highest sampling consensus in KIRC. Additionally, LINC02634 RNA expression shows 6,607 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight BLCA, KIRC, and STAD as cancer lineages where LINC02634 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 LINC02634 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02634 survival associations across molecular data types. LINC02634 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC02634 RNA expression–survival associations across cancer types. High LINC02634 expression shows unfavorable associations in BLCA, UVM, STAD, LAML and PAAD, but favorable associations in COAD. The BLCA 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 BLCA as the clearest survival context for LINC02634 RNA expression.
This table summarizes LINC02634 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 7. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02634. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02634 shows lower tumor expression in BRCA, STAD, UCEC and LUSC and higher tumor expression in KIRC and THCA. The KIRC box plot shows higher LINC02634 RNA expression in tumor versus normal tissue (log2 FC = +0.116, t-test p = .010).
This table shows molecular features associated with LINC02634 in patient tissues and cancer cell lines. In patient samples, LINC02634 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
