GABA type A receptor associated protein like 1Genealiases: APG8-LIKE · APG8L · ATG8 · ATG8B · ATG8L · GEC1
Q-omics provides the consensus-scored GABARAPL1 profile across patient tissues and cancer cell-line models. GABARAPL1 expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, GABARAPL1 is differentially expressed in 14, with the highest sampling consensus in KIRC. Additionally, GABARAPL1 RNA expression shows 19,522 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight UVM, KIRC, and GBM as cancer lineages where GABARAPL1 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 GABARAPL1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes GABARAPL1 survival associations across molecular data types. GABARAPL1 RNA expression shows survival associations in the most cancer types (22), followed by mutation status (1) and mass-spec protein abundance (5). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible GABARAPL1 RNA expression–survival associations across cancer types. High GABARAPL1 expression shows unfavorable associations in STAD, but favorable associations in UVM, LIHC, LGG, SKCM and KIRC. The UVM Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify UVM as the clearest survival context for GABARAPL1 RNA expression.
This table summarizes GABARAPL1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 14, while mass-spec protein shows differences in 3. The strongest signals are observed in KIRC for RNA and CCRCC for protein.
This table ranks reproducible tumor–normal expression differences for GABARAPL1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. GABARAPL1 shows lower tumor expression in KIRC, LUAD, THCA, BLCA, COAD and KIRP. The KIRC box plot shows higher GABARAPL1 RNA expression in normal versus tumor tissue (log2 FC = −1.700, t-test p < 0.001).
This table shows molecular features associated with GABARAPL1 in patient tissues and cancer cell lines. In patient samples, GABARAPL1 shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set. In cancer cell lines, GABARAPL1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in BLOOD_Lymphoma, while CRISPR and shRNA rows add functional-dependency signals in CNS and LARGE_INTESTINE.
