SWAP70
Switch-associated protein 70
Also known as: KIAA0640, SWAP-70, SWP70_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UH65
- Gene
- SWAP70
- Ensembl
- ENSG00000133789
- Chromosome
- 11
- Canonical length
- 585 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Actin filaments
OverviewNCBI Gene
Enables cadherin binding activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to act upstream of or within isotype switching. Located in actin cytoskeleton; cytoplasm; and plasma membrane. Is active in postsynapse. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
585 residues, UniProt reviewed canonical sequence.
>Q9UH65|SWAP70
1 MGSLKEELLK AIWHAFTALD QDHSGKVSKS QLKVLSHNLC TVLKVPHDPV ALEEHFRDDD
61 EGPVSNQGYM PYLNRFILEK VQDNFDKIEF NRMCWTLCVK KNLTKNPLLI TEEDAFKIWV
121 IFNFLSEDKY PLIIVSEEIE YLLKKLTEAM GGGWQQEQFE HYKINFDDSK NGLSAWELIE
181 LIGNGQFSKG MDRQTVSMAI NEVFNELILD VLKQGYMMKK GHRRKNWTER WFVLKPNIIS
241 YYVSEDLKDK KGDILLDENC CVESLPDKDG KKCLFLVKCF DKTFEISASD KKKKQEWIQA
301 IHSTIHLLKL GSPPPHKEAR QRRKELRKKQ LAEQEELERQ MKELQAANES KQQELEAVRK
361 KLEEAASRAA EEEKKRLQTQ VELQARFSTE LEREKLIRQQ MEEQVAQKSS ELEQYLQRVR
421 ELEDMYLKLQ EALEDERQAR QDEETVRKLQ ARLLEEESSK RAELEKWHLE QQQAIQTTEA
481 EKQELENQRV LKEQALQEAM EQLEQLELER KQALEQYEEV KKKLEMATNK TKSWKDKVAH
541 HEGLIRLIEP GSKNPHLITN WGPAAFTEAE LEEREKNWKE KKTTELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SWAP70 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 71 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 71 nTPM
- lymph node: 62 nTPM
- spleen: 56 nTPM
- adipose tissue: 37 nTPM
- placenta: 37 nTPM
- appendix: 35 nTPM
Single-cell type
- b-cells: 424 nCPM
- vascular endothelial cells: 322 nCPM
- extravillous trophoblasts: 275 nCPM
- syncytiotrophoblasts: 254 nCPM
- endometrial ciliated cells: 243 nCPM
- microglia: 229 nCPM
Immune cell
- naive B-cell: 85 nTPM
- memory B-cell: 81 nTPM
- eosinophil: 49 nTPM
- non-classical monocyte: 30 nTPM
- basophil: 20 nTPM
- intermediate monocyte: 14 nTPM
Brain region
- choroid plexus: 28 nTPM
- medulla oblongata: 28 nTPM
- spinal cord: 27 nTPM
- white matter: 26 nTPM
- pons: 25 nTPM
- thalamus: 23 nTPM
ReferencesPubMed · IEDB
Publications for SWAP70 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
2 publications
- Seroreactivity against PTEN-induced putative kinase 1 (PINK1) in Turkish patients with Behçet's disease.
2009 · Clin Exp Rheumatol · RCR 0.5 · 15 citations - Switch-associated protein 70 antibodies in multiple sclerosis: relationship between increased serum levels and clinical relapse.
2012 · Inflamm Res · RCR 0.2 · 7 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 0.47
- gnomAD pLI
- 0.05
- gnomAD missense Z
- 1.83
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin filament bundle assembly
- isotype switching
- negative regulation of actin filament depolymerization
- negative regulation of cell-cell adhesion mediated by integrin
- positive regulation of actin filament bundle assembly
- positive regulation of cytosolic calcium ion concentration
- positive regulation of mast cell chemotaxis
- regulation of protein localization
- regulation of small GTPase mediated signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SWAP70 as an antibody target. Whether an autoantibody or antibody against SWAP70 could matter depends on whether native SWAP70 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SWAP70 is annotated at the cell surface, where native SWAP70 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SWAP70 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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