IGFBP2
Insulin-like growth factor-binding protein 2
Also known as: IBP2, IBP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P18065
- Gene
- IGFBP2
- Ensembl
- ENSG00000115457
- Chromosome
- 2
- Canonical length
- 325 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Endoplasmic reticulum
- Secretome location
- Secreted to blood
OverviewNCBI Gene
The protein encoded by this gene is one of six similar proteins that bind insulin-like growth factors I and II (IGF-I and IGF-II). The encoded protein can be secreted into the bloodstream, where it binds IGF-I and IGF-II with high affinity, or it can remain intracellular, interacting with many different ligands. High expression levels of this protein promote the growth of several types of tumors and may be predictive of the chances of recovery of the patient. Several transcript variants, one encoding a secreted isoform and the others encoding nonsecreted isoforms, have been found for this gene. [provided by RefSeq, Sep 2015]
Canonical amino-acid sequenceUniProt
325 residues, UniProt reviewed canonical sequence.
>P18065|IGFBP2
1 MLPRVGCPAL PLPPPPLLPL LLLLLGASGG GGGARAEVLF RCPPCTPERL AACGPPPVAP
61 PAAVAAVAGG ARMPCAELVR EPGCGCCSVC ARLEGEACGV YTPRCGQGLR CYPHPGSELP
121 LQALVMGEGT CEKRRDAEYG ASPEQVADNG DDHSEGGLVE NHVDSTMNML GGGGSAGRKP
181 LKSGMKELAV FREKVTEQHR QMGKGGKHHL GLEEPKKLRP PPARTPCQQE LDQVLERIST
241 MRLPDERGPL EHLYSLHIPN CDKHGLYNLK QCKMSLNGQR GECWCVNPNT GKLIQGAPTI
301 RGDPECHLFY NEQQEARGVH TQRMQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IGFBP2 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.53
- Highest tissue expression
- 1,281 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 1,281 nTPM
- pancreas: 901 nTPM
- liver: 556 nTPM
- stomach: 460 nTPM
- choroid plexus: 403 nTPM
- spleen: 385 nTPM
Single-cell type
- breast myoepithelial cells: 1,706 nCPM
- parietal cells: 1,632 nCPM
- endometrial stromal cells: 1,022 nCPM
- respiratory ciliated cells: 826 nCPM
- hepatocytes: 823 nCPM
- gastric chief cells: 681 nCPM
Immune cell
- NK-cell: 0.3 nTPM
- MAIT T-cell: 0.1 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- choroid plexus: 239 nTPM
- midbrain: 29 nTPM
- cerebral cortex: 28 nTPM
- medulla oblongata: 24 nTPM
- hypothalamus: 17 nTPM
- thalamus: 16 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about IGFBP2.
Disease | ImmuneIEDB
Conditions an epitope on IGFBP2 was assayed in.
- breast cancer T cell
ReferencesPubMed · IEDB
Publications for IGFBP2 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
3 publications
- Autoantibodies against insulin-like growth factor‑binding protein-2 as a serological biomarker in the diagnosis of lung cancer.
2013 · Int J Oncol · RCR 1.1 · 34 citations - Elevated serum antibodies against insulin-like growth factor-binding protein-2 allow detecting early-stage cancers: evidences from glioma and colorectal carcinoma studies.
2012 · Ann Oncol · RCR 0.7 · 24 citations - Prognostic Value of Circulating IGFBP2 and Related Autoantibodies in Children with Metastatic Rhabdomyosarcomas.
2020 · Diagnostics (Basel) · RCR 0.4 · 8 citations
Reference: T cellIEDB
1 publication
- Elimination of IL-10-inducing T-helper epitopes from an IGFBP-2 vaccine ensures potent antitumor activity.
2014 · Cancer Res · RCR 1 · 39 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. IEDB — curated epitope assays from the Immune Epitope Database (Vita et al., Nucleic Acids Research 2019). 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)
- 0.82
- gnomAD pLI
- 0.12
- gnomAD missense Z
- 1.71
- DepMap mean gene effect
- 0.05
- 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
- cellular response to hormone stimulus
- female pregnancy
- negative regulation of canonical Wnt signaling pathway
- osteoblast differentiation
- positive regulation of activated T cell proliferation
- regulation of insulin-like growth factor receptor signaling pathway
- response to estradiol
- response to estrogen
- response to glucocorticoid
- response to mechanical stimulus
- response to nutrient
- response to retinoic acid
- response to xenobiotic stimulus
Molecular functions
- insulin-like growth factor I binding
- insulin-like growth factor II binding
- receptor ligand inhibitor activity
- signaling receptor binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Thyroglobulin type-1
- Insulin-like growth factor-binding protein, IGFBP
- Growth factor receptor cysteine-rich domain superfamily
- Insulin-like growth factor binding protein, N-terminal, Cys-rich conserved site
- Insulin-like growth factor-binding protein family 1-6, chordata
- Thyroglobulin type-1 superfamily
- Thyroglobulin type-1 repeat
- Insulin-like growth factor binding protein
- Insulin-like growth factor binding protein 2
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IGFBP2 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 IGFBP2 as an antibody target. Whether an autoantibody or antibody against IGFBP2 could matter depends on whether native IGFBP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IGFBP2 is annotated as secreted, so native IGFBP2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label IGFBP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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