Homo sapiens Protein: FGF12
Summary
InnateDB Protein IDBP-386666.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FGF12
Protein Name fibroblast growth factor 12
Synonyms FGF12B; FHF1;
Species Homo sapiens
Ensembl Protein ENSP00000397635
InnateDB Gene IDBG-69854 (FGF12)
Protein Structure
UniProt Annotation
Function Probably involved in nervous system development and function.
Subcellular Localization Nucleus {ECO:0000305}.
Disease Associations
Tissue Specificity Brain, eye and testis; highly expressed in embryonic retina, olfactory epithelium, olfactory bulb, and in a segmental pattern of the body wall; in adult olfactory bulb, less in cerebellum, deep cerebellar nuclei, cortex and multiple midbrain structures.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 12 experimentally validated interaction(s) in this database.
Experimentally validated
Total 12 [view]
Protein-Protein 12 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0008083 growth factor activity
GO:0008201 heparin binding
GO:0017080 sodium channel regulator activity
GO:0044325 ion channel binding
Biological Process
GO:0007165 signal transduction
GO:0007254 JNK cascade
GO:0007267 cell-cell signaling
GO:0007399 nervous system development
GO:0007507 heart development
GO:0008543 fibroblast growth factor receptor signaling pathway
GO:0086002 cardiac muscle cell action potential involved in contraction
GO:1902305 regulation of sodium ion transmembrane transport
GO:2000649 regulation of sodium ion transmembrane transporter activity
Cellular Component
GO:0005615 extracellular space
GO:0005634 nucleus
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 P61328
PhosphoSite PhosphoSite-P61328
TrEMBL C9JUK8
UniProt Splice Variant
Entrez Gene 2257
UniGene Hs.584758
RefSeq
HUGO HGNC:3668
OMIM 601513
CCDS CCDS46983
HPRD 03303
IMGT
EMBL AC026671 AC073363 AC079623 AC079847 AC128710 AK125307 AK312513 AK313671 BC022524 CH471052 U66197 U76381
GenPept AAB18786 AAB18913 AAH22524 BAG35414 BAG36423 BAG54181 EAW78084