Q-omics provides the consensus-scored GAPDHP44 profile across patient tissues and cancer cell-line models. GAPDHP44 expression is associated with patient survival in 23 of 34 cancer types, with the highest sampling consensus in MESO. Among the 18 cancer types available for tumor–normal comparison, GAPDHP44 is differentially expressed in 13, with the highest sampling consensus in KIRC. Additionally, GAPDHP44 RNA expression shows 14,382 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight MESO, KIRC, and GBM as cancer lineages where GAPDHP44 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 GAPDHP44 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes GAPDHP44 survival associations across molecular data types. GAPDHP44 RNA expression shows survival associations in the most cancer types (23). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible GAPDHP44 RNA expression–survival associations across cancer types. High GAPDHP44 expression shows unfavorable associations in MESO, KICH, LUAD, LIHC and KIRP, but favorable associations in READ. The MESO 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 MESO as the clearest survival context for GAPDHP44 RNA expression.
This table summarizes GAPDHP44 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 13. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for GAPDHP44. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. GAPDHP44 shows higher tumor expression in KIRC, LUAD, HNSC, LUSC, COAD and BRCA. The KIRC box plot shows higher GAPDHP44 RNA expression in tumor versus normal tissue (log2 FC = +0.543, t-test p < 0.001).
This table shows molecular features associated with GAPDHP44 in patient tissues and cancer cell lines. In patient samples, GAPDHP44 shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set.
