ITGB2
Integrin beta-2
Also known as: CD18, ITB2_HUMAN, LFA-1, MAC-1, MFI7
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P05107
- Gene
- ITGB2
- Ensembl
- ENSG00000160255
- Chromosome
- 21
- Canonical length
- 769 aa
- Protein class
- CD markers, Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Plasma membrane,Rods & Rings
OverviewNCBI Gene
This gene encodes an integrin beta chain, which combines with multiple different alpha chains to form different integrin heterodimers. Integrins are integral cell-surface proteins that participate in cell adhesion as well as cell-surface mediated signalling. The encoded protein plays an important role in immune response and defects in this gene cause leukocyte adhesion deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Canonical amino-acid sequenceUniProt
769 residues, UniProt reviewed canonical sequence.
>P05107|ITGB2
1 MLGLRPPLLA LVGLLSLGCV LSQECTKFKV SSCRECIESG PGCTWCQKLN FTGPGDPDSI
61 RCDTRPQLLM RGCAADDIMD PTSLAETQED HNGGQKQLSP QKVTLYLRPG QAAAFNVTFR
121 RAKGYPIDLY YLMDLSYSML DDLRNVKKLG GDLLRALNEI TESGRIGFGS FVDKTVLPFV
181 NTHPDKLRNP CPNKEKECQP PFAFRHVLKL TNNSNQFQTE VGKQLISGNL DAPEGGLDAM
241 MQVAACPEEI GWRNVTRLLV FATDDGFHFA GDGKLGAILT PNDGRCHLED NLYKRSNEFD
301 YPSVGQLAHK LAENNIQPIF AVTSRMVKTY EKLTEIIPKS AVGELSEDSS NVVHLIKNAY
361 NKLSSRVFLD HNALPDTLKV TYDSFCSNGV THRNQPRGDC DGVQINVPIT FQVKVTATEC
421 IQEQSFVIRA LGFTDIVTVQ VLPQCECRCR DQSRDRSLCH GKGFLECGIC RCDTGYIGKN
481 CECQTQGRSS QELEGSCRKD NNSIICSGLG DCVCGQCLCH TSDVPGKLIY GQYCECDTIN
541 CERYNGQVCG GPGRGLCFCG KCRCHPGFEG SACQCERTTE GCLNPRRVEC SGRGRCRCNV
601 CECHSGYQLP LCQECPGCPS PCGKYISCAE CLKFEKGPFG KNCSAACPGL QLSNNPVKGR
661 TCKERDSEGC WVAYTLEQQD GMDRYLIYVD ESRECVAGPN IAAIVGGTVA GIVLIGILLL
721 VIWKALIHLS DLREYRRFEK EKLKSQWNND NPLFKSATTT VMNPKFAESLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ITGB2 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
- 1
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 343 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 343 nTPM
- appendix: 163 nTPM
- lymph node: 155 nTPM
- spleen: 135 nTPM
- thymus: 80 nTPM
- lung: 73 nTPM
Single-cell type
- neutrophils: 726 nCPM
- monocytes: 614 nCPM
- hofbauer cells: 523 nCPM
- cdc: 400 nCPM
- monocyte progenitors: 358 nCPM
- macrophages: 345 nCPM
Immune cell
- total PBMC: 3,032 nTPM
- classical monocyte: 1,850 nTPM
- neutrophil: 1,390 nTPM
- eosinophil: 1,226 nTPM
- non-classical monocyte: 1,188 nTPM
- intermediate monocyte: 1,144 nTPM
Brain region
- white matter: 120 nTPM
- medulla oblongata: 76 nTPM
- pons: 73 nTPM
- thalamus: 71 nTPM
- spinal cord: 64 nTPM
- midbrain: 44 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ITGB2.
Disease | AllUniProt
Conditions ITGB2 is implicated in, by any mechanism.
- Leukocyte adhesion deficiency 1 (LAD1) MIM:116920
Disease | GeneticClinVar
84 pathogenic / likely-pathogenic of 932 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Leukocyte adhesion deficiency 1
- ITGB2-related disorder
- Inborn genetic diseases
- Leukocyte adhesion deficiency 3
- Glioma susceptibility 1
ReferencesPubMed · IEDB
Publications for ITGB2 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
4 publications
- Effect of tumor necrosis factor-induced integrin activation on Fc gamma receptor II-mediated signal transduction: relevance for activation of neutrophils by anti-proteinase 3 or anti-myeloperoxidase antibodies.
1995 · Blood · RCR 3.6 · 136 citations - Anti-neutrophil cytoplasm antibodies (ANCA) increase neutrophil adhesion to cultured human endothelium.
1993 · Adv Exp Med Biol · RCR 0.9 · 29 citations - Increased membrane expression of proteinase 3 during neutrophil adhesion in the presence of anti proteinase 3 antibodies.
2007 · J Am Soc Nephrol · RCR 0.6 · 27 citations - [Analysis of complement-mediated phagocytosis in systemic lupus erythematosus model mice, NZB/W F1].
1994 · Kansenshogaku Zasshi
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)
- 0.99
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.77
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
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
- amyloid-beta clearance
- apoptotic process
- cell adhesion
- cell adhesion mediated by integrin
- cell-cell adhesion
- cell-cell adhesion via plasma-membrane adhesion molecules
- cell-cell signaling
- cell-matrix adhesion
- cellular extravasation
- cellular response to low-density lipoprotein particle stimulus
- endodermal cell differentiation
- endothelial cell migration
- heterotypic cell-cell adhesion
- inflammatory response
- integrin-mediated signaling pathway
- leukocyte cell-cell adhesion
- leukocyte migration involved in inflammatory response
- microglial cell activation
- negative regulation of dopamine metabolic process
- neutrophil chemotaxis
- neutrophil migration
- phagocytosis, engulfment
- positive regulation of angiogenesis
- positive regulation of leukocyte adhesion to vascular endothelial cell
- positive regulation of neutrophil degranulation
- positive regulation of nitric oxide biosynthetic process
- positive regulation of protein targeting to membrane
- positive regulation of superoxide anion generation
- receptor clustering
- receptor internalization
- receptor-mediated endocytosis
- regulation of cell shape
- regulation of peptidyl-tyrosine phosphorylation
Molecular functions
- amyloid-beta binding
- cell adhesion molecule binding
- complement component C3b binding
- heat shock protein binding
- ICAM-3 receptor activity
- integrin binding
- metal ion binding
- protein kinase binding
Cellular components
- cell surface
- external side of plasma membrane
- extracellular exosome
- extracellular vesicle
- ficolin-1-rich granule membrane
- focal adhesion
- integrin alphaD-beta2 complex
- integrin alphaL-beta2 complex
- integrin alphaM-beta2 complex
- integrin alphaX-beta2 complex
- integrin complex
- membrane
- plasma membrane
- plasma membrane raft
- receptor complex
- specific granule membrane
- tertiary granule membrane
Protein domainsUniProt · Pfam · InterPro
- Integrin beta subunit, VWA domain
- Integrin beta subunit, tail
- Integrin beta subunit, cytoplasmic domain
- Integrin beta subunit
- PSI domain
- Integrin domain superfamily
- Integrin beta N-terminal
- Integrin beta tail domain superfamily
- von Willebrand factor A-like domain superfamily
- Integrin beta, epidermal growth factor-like domain 2
- Integrins beta, I-EGF domain, conserved site
- Integrin beta chain VWA domain
- Integrin beta tail domain
- Integrin beta cytoplasmic domain
- Integrin plexin domain
- Integrin EGF domain
- Integrin beta-2 superfamily
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ITGB2 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 ITGB2 as an antibody target. Whether an autoantibody or antibody against ITGB2 could matter depends on whether native ITGB2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ITGB2 is annotated at the cell surface, where native ITGB2 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 ITGB2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...