GABARAPL1
Gamma-aminobutyric acid receptor-associated protein-like 1
Also known as: APG8L, ATG8B, ATG8L, GBRL1_HUMAN, gec1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H0R8
- Gene
- GABARAPL1
- Ensembl
- ENSG00000139112
- Chromosome
- 12
- Canonical length
- 117 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Plasma membrane,Primary cilium,Basal body,Cytosol
OverviewNCBI Gene
Enables Tat protein binding activity; phospholipid binding activity; and ubiquitin protein ligase binding activity. Predicted to be involved in cellular response to nitrogen starvation and macroautophagy. Located in several cellular components, including autophagosome; ciliary basal body; and mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
117 residues, UniProt reviewed canonical sequence.
>Q9H0R8|GABARAPL1
1 MKFQYKEDHP FEYRKKEGEK IRKKYPDRVP VIVEKAPKAR VPDLDKRKYL VPSDLTVGQF
61 YFLIRKRIHL RPEDALFFFV NNTIPPTSAT MGQLYEDNHE EDYFLYVAYS DESVYGKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GABARAPL1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 377 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 377 nTPM
- heart muscle: 319 nTPM
- cerebral cortex: 305 nTPM
- kidney: 303 nTPM
- retina: 303 nTPM
- choroid plexus: 278 nTPM
Single-cell type
- syncytiotrophoblasts: 1,338 nCPM
- cytotrophoblasts: 381 nCPM
- early spermatids: 323 nCPM
- neutrophils: 317 nCPM
- epididymal clear cells: 253 nCPM
- parietal cells: 246 nCPM
Immune cell
- neutrophil: 62 nTPM
- basophil: 54 nTPM
- eosinophil: 43 nTPM
- gdT-cell: 27 nTPM
- NK-cell: 23 nTPM
- memory CD8 T-cell: 16 nTPM
Brain region
- cerebral cortex: 476 nTPM
- hypothalamus: 363 nTPM
- pons: 335 nTPM
- medulla oblongata: 315 nTPM
- white matter: 312 nTPM
- basal ganglia: 297 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.5
- gnomAD pLI
- 0.84
- gnomAD missense Z
- 1.19
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- autophagosome assembly
- autophagosome maturation
- cellular response to nitrogen starvation
- glycophagy
- mitophagy
Molecular functions
- beta-tubulin binding
- cargo adaptor activity
- GABA receptor binding
- phosphatidylethanolamine binding
- phospholipid binding
- Tat protein binding
- ubiquitin protein ligase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GABARAPL1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GABARAPL1 as an antibody target. Whether an autoantibody or antibody against GABARAPL1 could matter depends on whether native GABARAPL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GABARAPL1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label GABARAPL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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