Gene

IGF2BP1

Species
Homo sapiens
Symbol
IGF2BP1
Name
insulin like growth factor 2 mRNA binding protein 1
Synonyms
  • coding region determinant-binding protein
  • CRD-BP
Biotype
protein coding gene
Automated Description
Enables N6-methyladenosine-containing RNA reader activity; mRNA binding activity; and translation regulator activity. Involved in post-transcriptional regulation of gene expression. Located in cytoplasmic ribonucleoprotein granule; cytosol; and nucleoplasm. Part of CRD-mediated mRNA stability complex and ribonucleoprotein complex.
RGD Description
This gene encodes a member of the insulin-like growth factor 2 mRNA-binding protein family. The protein encoded by this gene contains four K homology domains and two RNA recognition motifs. It functions by binding to the mRNAs of certain genes, including insulin-like growth factor 2, beta-actin and beta-transducin repeat-containing protein, and regulating their translation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR10288
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Mus musculusIgf2bp110 of 10YesYes  
Rattus norvegicusIgf2bp110 of 10YesYes  
Danio rerioigf2bp19 of 10YesYes  
Drosophila melanogasterImp9 of 9YesYes   
Caenorhabditis elegansimph-18 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
IGF2BP3159184747 of 8  
IGF2BP2260978657 of 8  
KHSRP349938243 of 8  
NOVA1452235223 of 8  
NOVA2548736243 of 8  
HNRNPK650136184 of 8  
FUBP3743741243 of 8  
FUBP1844341233 of 8  
PCBP4941234223 of 8  
PCBP11036541233 of 8  
PCBP21140040202 of 8  
PCBP31223043273 of 8  

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
No data available

Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume
Species
Gene
Association
Disease Qualifier
Disease
Evidence
Source
Based On
References
No records match query. Try removing filters.
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    Alleles and Variants

    Genome location
    Assembly version
    GRCh38
    Viewer Help
    Data currently unavailable; sequence viewer under construction
    Allele/Variant Symbol
    Allele Synonyms
    Category
    Variant
    Variant type
    Molecular consequence
    Has Disease Annotations
    Has Phenotype Annotations
    NC_000017.11:g.49040021C>Tvariant
    SNP
    • missense variant
    NC_000017.11:g.49042318G>Avariant
    SNP
    • missense variant
    NC_000017.11:g.49038273G>Avariant
    SNP
    • synonymous variant
    NC_000017.11:g.49038421C>Tvariant
    SNP
    • missense variant
    NC_000017.11:g.49039981C>Tvariant
    SNP
    • synonymous variant
    NC_000017.11:g.49043504C>Avariant
    SNP
    • missense variant
    NC_000017.11:g.49043976G>Avariant
    SNP
    • missense variant
    NC_000017.11:g.49049433C>Tvariant
    SNP
    • missense variant
    NC_000017.11:g.49055457T>Cvariant
    SNP
    • 3 prime UTR variant
    NC_000017.11:g.49042376G>Avariant
    SNP
    • missense variant
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    Transgenic Alleles

    Species
    (carrying the transgene)
    Allele symbol
    Transgenic construct
    Expressed components
    Knock-down targets
    Regulatory regions
    Has Disease Annotations
    Has Phenotype Annotations
    Drosophila melanogasterHsap\IGF2BP1UAS.GFP
    • UASt
    Drosophila melanogasterHsap\IGF2BP1UAS.Tag:HA
    • UASt
    Drosophila melanogasterHsap\IGF2BP1UAS.cFa
    • UASt
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    Models

    No data available

    Sequence Feature Viewer

    Genome location
    Assembly version
    GRCh38
    Viewer Help
    Data currently unavailable; sequence viewer under construction

    Sequence Details

    Transcript: Mode:

    Expression

    Primary Sources
    None
    Other Sources
    Must provide at least one subject
    Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

    Molecular Interactions

    518 interactor genes based on 648 annotations
    IGF2BP1 molecule type
    Interactor gene
    Interactor species
    Interactor molecule type
    Detection methods
    Source
    Reference
    protein
    AATFHomo sapiens
    protein
    • affinity chromatography technology
    PMID:31363146
    protein
    ACE2Homo sapiens
    protein
    • affinity chromatography technology
    PMID:36057605
    protein
    ACE2Homo sapiens
    protein
    • affinity chromatography technology
    PMID:38245532
    protein
    ACE2Homo sapiens
    protein
    • affinity chromatography technology
    PMID:38245532
    protein
    ACTC1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:30890647
    protein
    AGO1Homo sapiens
    protein
    • proximity labelling technology
    PMID:29395067
    protein
    AGO1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:17932509
    protein
    AGO2Homo sapiens
    protein
    • proximity labelling technology
    PMID:29395067
    protein
    AGO2Homo sapiens
    protein
    • affinity chromatography technology
    PMID:17932509
    protein
    AGO4Homo sapiens
    protein
    • affinity chromatography technology
    PMID:19167051
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    Genetic Interactions

    IGF2BP1 role
    IGF2BP1 genetic perturbation
    Interactor gene
    Interactor species
    Interactor role
    Interactor genetic perturbation
    Interaction type
    Phenotype or trait
    Source
    Reference
    unspecified role
    ARFGAP2Homo sapiens
    unspecified role
    positive genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    ARIH2Homo sapiens
    unspecified role
    positive genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    B3GNT2Homo sapiens
    unspecified role
    positive genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    BMI1Homo sapiens
    unspecified role
    negative genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    CAND1Homo sapiens
    unspecified role
    positive genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    CUL5Homo sapiens
    unspecified role
    positive genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    DCAF7Homo sapiens
    unspecified role
    negative genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    EP300Homo sapiens
    unspecified role
    positive genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    HDAC8Homo sapiens
    unspecified role
    negative genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
    unspecified role
    HMGCRHomo sapiens
    unspecified role
    negative genetic interaction (sensu BioGRID)
    • Growth abnormality
    PMID:28319085
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