ADAP1
Arf-GAP with dual PH domain-containing protein 1
Also known as: ADAP1_HUMAN, CENTA1, GCS1L
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75689
- Gene
- ADAP1
- Ensembl
- ENSG00000105963
- Chromosome
- 7
- Canonical length
- 374 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
Enables GTPase activator activity. Predicted to be involved in cell surface receptor signaling pathway. Located in cytosol; nucleus; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
374 residues, UniProt reviewed canonical sequence.
>O75689|ADAP1
1 MAKERRRAVL ELLQRPGNAR CADCGAPDPD WASYTLGVFI CLSCSGIHRN IPQVSKVKSV
61 RLDAWEEAQV EFMASHGNDA ARARFESKVP SFYYRPTPSD CQLLREQWIR AKYERQEFIY
121 PEKQEPYSAG YREGFLWKRG RDNGQFLSRK FVLTEREGAL KYFNRNDAKE PKAVMKIEHL
181 NATFQPAKIG HPHGLQVTYL KDNSTRNIFI YHEDGKEIVD WFNALRAARF HYLQVAFPGA
241 GDADLVPKLS RNYLKEGYME KTGPKQTEGF RKRWFTMDDR RLMYFKDPLD AFARGEVFIG
301 SKESGYTVLH GFPPSTQGHH WPHGITIVTP DRKFLFACET ESDQREWVAA FQKAVDRPML
361 PQEYAVEAHF KHKPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ADAP1 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)
- 0.25
- Highest tissue expression
- 131 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 131 nTPM
- cerebral cortex: 127 nTPM
- hippocampal formation: 124 nTPM
- amygdala: 109 nTPM
- midbrain: 86 nTPM
- basal ganglia: 77 nTPM
Single-cell type
- oocytes: 286 nCPM
- colonocytes: 76 nCPM
- oligodendrocytes: 60 nCPM
- foveolar cells: 47 nCPM
- enterocytes: 43 nCPM
- monocytes: 42 nCPM
Immune cell
- non-classical monocyte: 12 nTPM
- intermediate monocyte: 7.3 nTPM
- classical monocyte: 6.5 nTPM
- gdT-cell: 6 nTPM
- memory CD8 T-cell: 5.5 nTPM
- myeloid DC: 5.1 nTPM
Brain region
- white matter: 157 nTPM
- cerebral cortex: 127 nTPM
- medulla oblongata: 118 nTPM
- midbrain: 116 nTPM
- hippocampal formation: 108 nTPM
- cerebellum: 104 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)
- 0.44
- gnomAD pLI
- 0.53
- gnomAD missense Z
- 0.89
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
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
Molecular functions
- GTPase activator activity
- inositol 1,3,4,5 tetrakisphosphate binding
- phosphatidylinositol bisphosphate binding
- phosphatidylinositol-3,4,5-trisphosphate binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ADAP1 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 ADAP1 as an antibody target. Whether an autoantibody or antibody against ADAP1 could matter depends on whether native ADAP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ADAP1 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 ADAP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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