IGF2BP2
Insulin-like growth factor 2 mRNA-binding protein 2
Also known as: IF2B2_HUMAN, IMP-2, p62
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y6M1
- Gene
- IGF2BP2
- Ensembl
- ENSG00000073792
- Chromosome
- 3
- Canonical length
- 599 aa
- Protein class
- Human disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
This gene encodes a protein that binds the 5' UTR of insulin-like growth factor 2 (IGF2) mRNA and regulates its translation. It plays an important role in metabolism and variation in this gene is associated with susceptibility to diabetes. Alternative splicing and promoter usage results in multiple transcript variants. Related pseudogenes are found on several chromosomes. [provided by RefSeq, Sep 2016]
Canonical amino-acid sequenceUniProt
599 residues, UniProt reviewed canonical sequence.
>Q9Y6M1|IGF2BP2
1 MMNKLYIGNL SPAVTADDLR QLFGDRKLPL AGQVLLKSGY AFVDYPDQNW AIRAIETLSG
61 KVELHGKIME VDYSVSKKLR SRKIQIRNIP PHLQWEVLDG LLAQYGTVEN VEQVNTDTET
121 AVVNVTYATR EEAKIAMEKL SGHQFENYSF KISYIPDEEV SSPSPPQRAQ RGDHSSREQG
181 HAPGGTSQAR QIDFPLRILV PTQFVGAIIG KEGLTIKNIT KQTQSRVDIH RKENSGAAEK
241 PVTIHATPEG TSEACRMILE IMQKEADETK LAEEIPLKIL AHNGLVGRLI GKEGRNLKKI
301 EHETGTKITI SSLQDLSIYN PERTITVKGT VEACASAEIE IMKKLREAFE NDMLAVNQQA
361 NLIPGLNLSA LGIFSTGLSV LSPPAGPRGA PPAAPYHPFT THSGYFSSLY PHHQFGPFPH
421 HHSYPEQEIV NLFIPTQAVG AIIGKKGAHI KQLARFAGAS IKIAPAEGPD VSERMVIITG
481 PPEAQFKAQG RIFGKLKEEN FFNPKEEVKL EAHIRVPSST AGRVIGKGGK TVNELQNLTS
541 AEVIVPRDQT PDENEEVIVR IIGHFFASQT AQRKIREIVQ QVKQQEQKYP QGVASQRSKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IGF2BP2 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)
- 0.37
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- retina: 21 nTPM
- small intestine: 15 nTPM
- placenta: 14 nTPM
- duodenum: 14 nTPM
- rectum: 14 nTPM
- stomach: 12 nTPM
Single-cell type
- endometrial luminal cells: 1,277 nCPM
- endometrial ciliated cells: 863 nCPM
- endometrial glandular cells: 803 nCPM
- endometrial secretory cells: 726 nCPM
- rod photoreceptor cells: 513 nCPM
- lacrimal acinar cells: 461 nCPM
Immune cell
- myeloid DC: 2.7 nTPM
- non-classical monocyte: 1.7 nTPM
- classical monocyte: 1.4 nTPM
- intermediate monocyte: 1.4 nTPM
- NK-cell: 0.7 nTPM
- total PBMC: 0.6 nTPM
Brain region
- cerebellum: 14 nTPM
- cerebral cortex: 6.3 nTPM
- medulla oblongata: 5 nTPM
- hypothalamus: 4.8 nTPM
- midbrain: 4.8 nTPM
- spinal cord: 3.6 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about IGF2BP2.
Disease | ImmuneIEDB
Conditions an epitope on IGF2BP2 was assayed in.
- melanoma T cell
- chronic lymphocytic leukemia T cell
- skin melanoma T cell
- acute myeloid leukemia T cell
Disease | AutoantibodyPubMed
Conditions in which antibodies against IGF2BP2 are reported. Each links to that disease's full target list.
Showing 3 of 4 — disease pages carrying at least 10 antigens.
ReferencesPubMed · IEDB
Publications for IGF2BP2 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
22 publications
- Autoantibodies against nucleoporin p62 constitute a novel marker of primary biliary cirrhosis.
1996 · Gastroenterology · RCR 1.9 · 78 citations - Profile and clinical significance of anti-nuclear envelope antibodies found in patients with primary biliary cirrhosis: a multicenter study.
2003 · J Autoimmun · RCR 1.9 · 73 citations - Autoantibodies to tumor-associated antigens as biomarkers in cancer immunodiagnosis.
2011 · Autoimmun Rev · RCR 1.7 · 63 citations - Cross reaction of antibodies to a glycine/alanine repeat sequence of Epstein-Barr virus nuclear antigen-1 with collagen, cytokeratin, and actin.
1991 · Ann Rheum Dis · RCR 1.7 · 48 citations - Two different subtypes of antimitochondrial antibodies are associated with primary biliary cirrhosis: identification and characterization by radioimmunoassay and immunoblotting.
1987 · Hepatology · RCR 1.6 · 46 citations
Show 17 more
- De-novo humoral immune responses to cancer-associated autoantigens during transition from chronic liver disease to hepatocellular carcinoma.
2001 · Clin Exp Immunol · RCR 1.5 · 66 citations - Autoimmune responses to mRNA binding proteins p62 and Koc in diverse malignancies.
2001 · Clin Immunol · RCR 1.3 · 60 citations - Reaction of antibodies to rheumatoid arthritis nuclear antigen with a synthetic peptide corresponding to part of Epstein-Barr nuclear antigen 1.
1988 · Ann Rheum Dis · RCR 1.1 · 35 citations - Preferential humoral immune response in prostate cancer to cellular proteins p90 and p62 in a panel of tumor-associated antigens.
2005 · Prostate · RCR 1.1 · 50 citations - The diversity expression of p62 in digestive system cancers.
2005 · Clin Immunol · RCR 0.8 · 44 citations - Overexpression of p62 Induces Autophagy and Promotes Proliferation, Migration and Invasion of Nasopharyngeal Carcinoma Cells through Promoting ERK Signaling Pathway.
2020 · Curr Cancer Drug Targets · RCR 0.8 · 16 citations - Antibodies to synthetic peptides from Epstein-Barr nuclear antigen-1 in sera of patients with early rheumatoid arthritis and in preillness sera.
1990 · J Rheumatol · RCR 0.8 · 30 citations - Humoral autoimmune response to IGF2 mRNA-binding protein (IMP2/p62) and its tissue-specific expression in colon cancer.
2013 · Scand J Immunol · RCR 0.8 · 28 citations - Antibodies in rheumatoid arthritis react specifically with the glycine alanine repeat sequence of Epstein-Barr nuclear antigen-1.
1989 · Rheumatol Int · RCR 0.6 · 24 citations - Autoantibodies to IGF-II mRNA binding protein p62 and overexpression of p62 in human hepatocellular carcinoma.
2002 · Autoimmun Rev · RCR 0.6 · 35 citations - Characterization of autoantibodies against components of the nuclear pore complexes: high frequency of anti-p62 nucleoporin antibodies.
2007 · Ann N Y Acad Sci · RCR 0.5 · 22 citations - [Sporadic adult-onset neuronal intranuclear inclusion disease with the main presentation of repeated cerebellar ataxia: a case study].
2016 · Rinsho Shinkeigaku · RCR 0.3 · 6 citations - Nucleoporin p62 antibodies in a case of mixed connective tissue disease.
2003 · Clin Diagn Lab Immunol · RCR 0.2 · 9 citations - Differential detection of nuclear envelope autoantibodies in primary biliary cirrhosis using routine and alternative methods.
2010 · BMC Gastroenterol · RCR 0.1 · 6 citations - Nuclear pore complex oxalate binding protein p62: expression in different kidney disorders.
2004 · Clin Chim Acta · RCR 0.1 · 5 citations - Nuclear Pore Protein p62 Autoantibodies in Systemic Lupus Erythematosus.
2010 · Open Rheumatol J · RCR 0.1 · 5 citations - Antibodies to synthetic peptide P62 corresponding to the major epitope of rheumatoid arthritis nuclear antigen in a west African population with rheumatoid arthritis.
1994 · Br J Rheumatol
Reference: T cellIEDB
2 publications
- Targeting of multiple tumor-associated antigens by individual T cell receptors during successful cancer immunotherapy.
2023 · Cell · RCR 9 · 114 citations - Optimized Peptide-MHC Multimer Protocols for Detection and Isolation of Autoimmune T-Cells.
2018 · Front Immunol · RCR 1.9 · 60 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)
- 0.43
- gnomAD pLI
- 0.24
- gnomAD missense Z
- 2.91
- DepMap mean gene effect
- -0.24
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- anatomical structure morphogenesis
- cold-induced thermogenesis
- CRD-mediated mRNA stabilization
- energy homeostasis
- mRNA transport
- negative regulation of translation
- nervous system development
- regulation of cytokine production
- RNA stabilization
Molecular functions
- mRNA 3'-UTR binding
- mRNA 5'-UTR binding
- N6-methyladenosine-containing RNA reader activity
- RNA binding
- translation regulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IGF2BP2 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 IGF2BP2 as an antibody target. Whether an autoantibody or antibody against IGF2BP2 could matter depends on whether native IGF2BP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IGF2BP2 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 IGF2BP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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