InnateDB Protein
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IDBP-62038.5
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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FGF3
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Protein Name
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fibroblast growth factor 3
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Synonyms
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HBGF-3; INT2;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000334122
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InnateDB Gene
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IDBG-62036 (FGF3)
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Protein Structure
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Function |
Plays an important role in the regulation of embryonic development, cell proliferation, and cell differentiation. Required for normal ear development. {ECO:0000269PubMed:8663044}.
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Subcellular Localization |
Secreted {ECO:0000305}.
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Disease Associations |
Deafness with labyrinthine aplasia, microtia and microdontia (LAMM) [MIM:610706]: Unique autosomal recessive syndrome characterized by type I microtia, microdontia, and profound congenital deafness associated with a complete absence of inner ear structures (Michel aplasia). {ECO:0000269PubMed:17236138, ECO:0000269PubMed:18435799}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
6
[view]
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Protein-Protein |
6
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR002209
Fibroblast growth factor family
IPR008996
Cytokine, IL-1-like
IPR028142
IL-1 family/FGF family
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PFAM |
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PRINTS |
PR00263
PR00262
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PIRSF |
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SMART |
SM00442
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TIGRFAMs |
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Modification |
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SwissProt |
P11487
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PhosphoSite |
PhosphoSite-P11487
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
2248
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UniGene |
Hs.37092
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RefSeq |
NP_005238
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HUGO |
HGNC:3681
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OMIM |
164950
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CCDS |
CCDS8195
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HPRD |
01289
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IMGT |
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EMBL |
BC113739
X14445
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GenPept |
AAI13740
CAA32615
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