Q-omics provides the consensus-scored LMX1A-AS2 profile across patient tissues and cancer cell-line models. LMX1A-AS2 expression is associated with patient survival in 13 of 34 cancer types, with the highest sampling consensus in STAD. Among the 18 cancer types available for tumor–normal comparison, LMX1A-AS2 is differentially expressed in 3, with the highest sampling consensus in BRCA. Additionally, LMX1A-AS2 RNA expression shows 7,276 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight STAD, BRCA, and TGCT as cancer lineages where LMX1A-AS2 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 LMX1A-AS2 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LMX1A-AS2 survival associations across molecular data types. LMX1A-AS2 RNA expression shows survival associations in the most cancer types (13). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LMX1A-AS2 RNA expression–survival associations across cancer types. High LMX1A-AS2 expression shows unfavorable associations in STAD, UVM, PAAD, MESO and READ, but favorable associations in UCS. The STAD 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 STAD as the clearest survival context for LMX1A-AS2 RNA expression.
This table summarizes LMX1A-AS2 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 LMX1A-AS2. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LMX1A-AS2 shows lower tumor expression in BRCA, COAD and THCA. The BRCA box plot shows higher LMX1A-AS2 RNA expression in normal versus tumor tissue (log2 FC = −0.038, t-test p < 0.001).
This table shows molecular features associated with LMX1A-AS2 in patient tissues and cancer cell lines. In patient samples, LMX1A-AS2 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
