DAPL1
Death-associated protein-like 1
Also known as: DAPL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A0PJW8
- Gene
- DAPL1
- Ensembl
- ENSG00000163331
- Chromosome
- 2
- Canonical length
- 107 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies,Microtubules
OverviewNCBI Gene
Predicted to enable ribosome binding activity; translation initiation factor binding activity; and translation repressor activity. Predicted to be involved in apoptotic signaling pathway; negative regulation of CD8-positive, alpha-beta T cell activation; and negative regulation of metabolic process. Predicted to act upstream of or within cell population proliferation and gene expression. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
107 residues, UniProt reviewed canonical sequence.
>A0PJW8|DAPL1
1 MANEVQDLLS PRKGGHPPAV KAGGMRISKK QEIGTLERHT KKTGFEKTSA IANVAKIQTL
61 DALNDALEKL NYKFPATVHM AHQKPTPALE KVVPLKRIYI IQQPRKCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DAPL1 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)
- 0.66
- Highest tissue expression
- 293 nTPM
Expression across tissuesHPA
Tissue
- skin: 293 nTPM
- esophagus: 234 nTPM
- epididymis: 186 nTPM
- retina: 107 nTPM
- vagina: 102 nTPM
- cervix: 94 nTPM
Single-cell type
- esophageal suprabasal cells: 1,285 nCPM
- esophageal basal cells: 930 nCPM
- ocular epithelial cells: 638 nCPM
- müller glia: 579 nCPM
- fallopian secretory cells: 412 nCPM
- suprabasal keratinocytes: 361 nCPM
Immune cell
- plasmacytoid DC: 1.1 nTPM
- basophil: 1 nTPM
- classical monocyte: 0.7 nTPM
- NK-cell: 0.7 nTPM
- intermediate monocyte: 0.5 nTPM
- eosinophil: 0.4 nTPM
Brain region
- cerebral cortex: 20 nTPM
- hypothalamus: 19 nTPM
- midbrain: 11 nTPM
- thalamus: 9.3 nTPM
- pons: 5.2 nTPM
- basal ganglia: 3.8 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)
- 1.88
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.58
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic signaling pathway
- cell differentiation
- cell population proliferation
- gene expression
- negative regulation of autophagy
- negative regulation of CD8-positive, alpha-beta T cell activation
- ribosome hibernation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DAPL1 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 DAPL1 as an antibody target. Whether an autoantibody or antibody against DAPL1 could matter depends on whether native DAPL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DAPL1 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 DAPL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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