Q-omics provides the consensus-scored MTND1P34 profile across patient tissues and cancer cell-line models. MTND1P34 expression is associated with patient survival in 13 of 34 cancer types, with the highest sampling consensus in READ. Among the 18 cancer types available for tumor–normal comparison, MTND1P34 is differentially expressed in 2, with the highest sampling consensus in STAD. Additionally, MTND1P34 RNA expression shows 7,438 significant protein co-abundance associations, with the highest sampling consensus in LSCC. Together, these results highlight READ, STAD, and LSCC as cancer lineages where MTND1P34 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 MTND1P34 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MTND1P34 survival associations across molecular data types. MTND1P34 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 MTND1P34 RNA expression–survival associations across cancer types. High MTND1P34 expression shows unfavorable associations in READ, PCPG, THCA and CESC, but favorable associations in BLCA and UCS. The READ 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 READ as the clearest survival context for MTND1P34 RNA expression.
This table summarizes MTND1P34 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in STAD for RNA.
This table ranks reproducible tumor–normal expression differences for MTND1P34. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MTND1P34 shows higher tumor expression in STAD and BRCA. The STAD box plot shows higher MTND1P34 RNA expression in tumor versus normal tissue (log2 FC = +0.181, t-test p = .002).
This table shows molecular features associated with MTND1P34 in patient tissues and cancer cell lines. In patient samples, MTND1P34 shows the broadest associations at the RNA and protein expression levels, with LSCC recurring as the lineage with the largest associated feature set.
