Species: Hu
Applications: WB
Host: Mouse Monoclonal
Species: Hu
Applications: Flow, ICC/IF
Host: Mouse Monoclonal
Species: Hu
Applications: IHC
Host: Mouse Monoclonal
Species: Hu
Applications: ELISA
Species: Hu
Applications: Bioactivity
Species: Hu
Applications: Bioactivity
Species: Hu
Applications: Bioactivity
Description
Fibroblast
growth factor receptor 2 (FGFR2) belongs to a family of type I transmembrane
tyrosine kinases which mediate the biological functions of FGFs that are
involved in a multitude of physiological and pathological cellular processes (1).
The FGFR family is comprised of 4
structurally conserved members (FGFR1-4) all possessing an extracellular
domain (ECD) with three immunoglobulin (Ig)-like domains, an acid-box region
containing a run of acidic residues between the IgI and IgII domains, a
transmembrane domain and cytoplasmic split tyrosine-kinase domain (1, 2). The ECD of
mature, full-length FGFR2 shares 95% amino acid sequence identity with mouse
FGFR2. Alternative splicing generates multiple forms of FGFR1-3, each with
unique signaling characteristics (1-3). For FGFR2, alternative splicing of
the ECD, specifically the IgIII domain, results in IIIb, or IIIc isoforms (4). The
FGFR splice variants also exhibit distinct and varying binding affinities for
different FGF ligands (2, 4). Specifically, FGFR2A (IIIc) binds most FGF ligands
but not the FGF10 subfamily, while FGFR2A (IIIc) binds only members of the FGF10 subfamily (5). FGFRs mediate
the FGF signaling cascade which regulate developmental processes including
cellular proliferation, differentiation, and migration, morphogenesis, and
patterning (6). FGFRs transduce the signals through three dominant pathways
including RAS/MAPK, PI3k/AKT, and PLC gamma (7). While FGFR2 is widely expressed in
many adult human tissues, isoform expression is tissue specific, with IIIb predominantly expressed in epithelial cells, while IIIc
is expressed in mesenchymal cells (5). FGFR2 signaling is critical for embryonic development, tissue repair, and regulation
of osteoblast function and bone growth (8). Mutations in FGFR2 or
misregulation of FGFR2 mediated signaling is found in multiple skeletal
dysplasias, with FGFR2A (IIIc) specifically
upregulated in several cancers including prostate, breast and pancreatic and is
proposed as a novel therapeutic target for colorectal carcinomas (6, 9).
Bioinformatics
| Uniprot |
|
| Product By Gene ID |
2263 |
| Alternate Names |
- BBDS;BEK;BFR-1;CD332;CEK3;CFD1;ECT1;Fibroblast growth factor receptor;Fibroblast growth factor receptor 2;JWS;KGFR;K-SAM;Receptor protein-tyrosine kinase;TK14;TK25
- FGF R2a
- FGFR2 alpha
|