Q-omics provides the consensus-scored FABP5P7 profile across patient tissues and cancer cell-line models. FABP5P7 expression is associated with patient survival in 23 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, FABP5P7 is differentially expressed in 9, with the highest sampling consensus in KIRC. Additionally, FABP5P7 RNA expression shows 15,846 significant gene co-expression associations, with the highest sampling consensus in ESCA. Together, these results highlight UVM, KIRC, and ESCA as cancer lineages where FABP5P7 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 FABP5P7 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes FABP5P7 survival associations across molecular data types. FABP5P7 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 FABP5P7 RNA expression–survival associations across cancer types. High FABP5P7 expression shows unfavorable associations in UVM, LUAD, LIHC, LGG, UCEC and SARC. The UVM 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 UVM as the clearest survival context for FABP5P7 RNA expression.
This table summarizes FABP5P7 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 9. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for FABP5P7. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. FABP5P7 shows lower tumor expression in LUAD and BRCA and higher tumor expression in KIRC, LIHC, HNSC and PRAD. The KIRC box plot shows higher FABP5P7 RNA expression in tumor versus normal tissue (log2 FC = +0.602, t-test p < 0.001).
This table shows molecular features associated with FABP5P7 in patient tissues and cancer cell lines. In patient samples, FABP5P7 shows the broadest associations at the RNA and protein expression levels, with ESCA recurring as the lineage with the largest associated feature set.
