fibroblast growth factor 9; FGF-9; Glia-activating factor; GAF; heparin-binding growth factor 9; HBGF-9 (FGF9)

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Function

Structure

Compartment

secreted

Expression

Glial cells

Pathology

  • defects in FGF9 are the cause of multiple synostoses syndrome type 3
  • the Asn-99 mutation is associated with impaired FGF signaling, as evidenced by diminished activity of the MAPK1/MAPK2 pathway & decreases CTNNB1 & MYC expression when compared with wild-type protein
  • binding of mutant protein to the receptor FGFR3 is severely impaired, although homodimerization of mutant to itself or wild-type is not detectably affected

More general terms

References

Database