Homo sapiens Protein: FGF9
Summary
InnateDB Protein IDBP-14812.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FGF9
Protein Name fibroblast growth factor 9 (glia-activating factor)
Synonyms FGF-9; GAF; HBFG-9; HBGF-9; SYNS3;
Species Homo sapiens
Ensembl Protein ENSP00000371790
InnateDB Gene IDBG-14810 (FGF9)
Protein Structure
UniProt Annotation
Function Plays an important role in the regulation of embryonic development, cell proliferation, cell differentiation and cell migration. May have a role in glial cell growth and differentiation during development, gliosis during repair and regeneration of brain tissue after damage, differentiation and survival of neuronal cells, and growth stimulation of glial tumors. {ECO:0000269PubMed:16597617, ECO:0000269PubMed:8663044}.
Subcellular Localization Secreted.
Disease Associations Multiple synostoses syndrome 3 (SYNS3) [MIM:612961]: A bone disease characterized by multiple progressive joint fusions that commonly involve proximal interphalangeal, tarsal-carpal, humeroradial and cervical spine joints. Additional features can include progressive conductive deafness and facial dysmorphism. {ECO:0000269PubMed:19589401}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Glial cells.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 4 [view]
Protein-Protein 4 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005104 fibroblast growth factor receptor binding
GO:0008083 growth factor activity
GO:0008201 heparin binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001525 angiogenesis
GO:0001649 osteoblast differentiation
GO:0002053 positive regulation of mesenchymal cell proliferation
GO:0002062 chondrocyte differentiation
GO:0006606 protein import into nucleus
GO:0007165 signal transduction
GO:0007173 epidermal growth factor receptor signaling pathway
GO:0007267 cell-cell signaling
GO:0008284 positive regulation of cell proliferation
GO:0008286 insulin receptor signaling pathway
GO:0008543 fibroblast growth factor receptor signaling pathway
GO:0008584 male gonad development
GO:0010628 positive regulation of gene expression
GO:0021762 substantia nigra development
GO:0030178 negative regulation of Wnt signaling pathway
GO:0030238 male sex determination
GO:0030324 lung development
GO:0030326 embryonic limb morphogenesis
GO:0030949 positive regulation of vascular endothelial growth factor receptor signaling pathway
GO:0038095 Fc-epsilon receptor signaling pathway
GO:0042472 inner ear morphogenesis
GO:0043410 positive regulation of MAPK cascade
GO:0045087 innate immune response
GO:0045880 positive regulation of smoothened signaling pathway
GO:0048011 neurotrophin TRK receptor signaling pathway
GO:0048015 phosphatidylinositol-mediated signaling
GO:0048505 regulation of timing of cell differentiation
GO:0048566 embryonic digestive tract development
GO:0048706 embryonic skeletal system development
GO:0050679 positive regulation of epithelial cell proliferation
GO:0051781 positive regulation of cell division
GO:0060045 positive regulation of cardiac muscle cell proliferation
GO:0060484 lung-associated mesenchyme development
GO:0090263 positive regulation of canonical Wnt signaling pathway
Cellular Component
GO:0005576 extracellular region
GO:0005604 basement membrane
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR002209 Fibroblast growth factor family
IPR008996 Cytokine, IL-1-like
IPR028142 IL-1 family/FGF family
PFAM
PRINTS PR00263
PR00262
PIRSF
SMART SM00442
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P31371
PhosphoSite PhosphoSite-P31371
TrEMBL
UniProt Splice Variant
Entrez Gene 2254
UniGene Hs.610336
RefSeq NP_002001
HUGO HGNC:3687
OMIM 600921
CCDS CCDS9298
HPRD 02951
IMGT
EMBL AK290792 AL139378 AY682094 BC069692 BC103978 BC103979 CH471075 D14838
GenPept AAH69692 AAI03979 AAI03980 AAT74624 BAA03572 BAF83481 CAC17692 EAX08316