Gene content    
IGFBP7 ( by HUGO)
Insulin-Like Growth Factor Binding Protein 7
Tumor suppressor gene
Insulin-Like Growth Factor Binding Protein 7
MAC25
Prostacyclin-Stimulating Factor
Tumor-Derived Adhesion Factor
IBP-7
IGFBP-7
IGFBP-rP1
PSF
TAF
IGF-Binding Protein 7
PGI2-Stimulating Factor
RAMSVPS
AGM
FSTL2
IGFBP-7v
IGFBPRP1
angiomodulin
Insulin-Like Growth Factor-Binding Protein 7
MAC25 Protein
NCBI: 4q12    Ensembl: 4q12
IBP7_HUMANSize: 282 amino acidsMass: 29130 Da

  • Subunit: May interact with VPS24/CHMP3; the relevance of such interaction however remains unclear Rna editing: Modified_positions=78, 95; Note=Partially edited. In the brain, position 78 is edited at about 55% and position 95 at about 31%
  • Function:
    UniProtKB/Swiss-Prot Summary: IBP7_HUMAN, Q16270 Function: Binds IGF-I and IGF-II with a relatively low affinity. Stimulates prostacyclin (PGI2) production. Stimulates cell adhesion
  • Similarity:
    Contains 1 Ig-like C2-type (immunoglobulin-like) domain
                          
    Contains 1 IGFBP N-terminal domain
                          
    Contains 1 Kazal-like domain [IMAGE]
  • Protein Domain/Family    
    Source ID Domain Name Type
    InterProIPR000867IGFBP-likeInsulin-like growth factor-binding protein, IGFBPDomain
    IPR002350Kazal_domProteinase inhibitor I1, KazalFamily
    IPR003599Ig_subImmunoglobulin subtypeDomain
    IPR007110Ig-like_domImmunoglobulin-likeDomain
    IPR009030Growth_fac_rcpt_N_domGrowth factor, receptorDomain
    IPR011390IGFBP_rP_mac25Insulin-like growth factor binding protein related protein (IGFBP-rP), MAC25Family
    IPR013098Ig_I-setImmunoglobulin I-setDomain
    BlocksIPB003599Immunoglobulin subtypeImmunoglobulin subtype
    IPB011497Protease inhibitorProtease inhibitor, Kazal-type

    Gene Ontology    
    Type Term Evidence Source Pub
    Biological Process cell adhesion IDA GOA 8117260
    negative regulation of cell proliferation TAS GOA 8939990
    Molecular Function protein binding IPI GOA 9388210

    Disorder & Mutation    
    Source Disease
    SWISS-PROTRetinal arterial macroaneurysm with supravalvular pulmonic stenosis (RAMSVPS) [MIM:614224]: An autosomal recessive condition characterized by the bilateral appearance of 'beading' along the major retinal arterial trunks, with the subsequent formation of macroaneurysms. Affected individuals also have supravalvular pulmonic stenosis, often requiring surgical correction. Note=The disease is caused by mutations affecting the gene represented in this entry

    IGFBP7 cross reference    
    PubMed OMIM Entrez Gene NCKU SNP Nucleotide UniProt Genome Data Viewer HomoloGene