Symbol Name ID

Fgfr2 fibroblast growth factor receptor 2 MGI:95523

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9 matching Alleles (1 Gene/Marker represented)

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                                    Allele Symbol
Name                                      Chr                 Synonyms                        Category                                                                                                                          Phenotypic Classes                                                                                                                                    Human Diseases                  

Fgfr2m1Sgg
fibroblast growth factor receptor 2; mutation 1, S G Gong                        7    Fgfr2W290R                             Chemically induced (ENU)  craniofacial, digestive/alimentary, embryogenesis, endocrine/exocrine, growth/size, hearing/vestibular/ear, limbs/digits/tail, mortality/aging, nervous system, renal/urinary, respiratory, skeleton, vision/eye                                   Crouzon Syndrome 123500                            

Fgfr2tm1.1Dsn
fibroblast growth factor receptor 2; targeted mutation 1.1, Clive Dickson
     7    Fgfr2b-, Fgfr2(IIIb)-, FgfR2-IIIb-Cre  Targeted (knock-out)      craniofacial, digestive/alimentary, endocrine/exocrine, growth/size, hearing/vestibular/ear, integument, limbs/digits/tail, mortality/aging, muscle, nervous system, pigmentation, renal/urinary, reproductive, respiratory, skeleton, vision/eye  Intestinal Atresia, Multiple 243150                

Fgfr2tm1Ewj
fibroblast growth factor receptor 2; targeted mutation 1, Ethylin Wang Jabs     7    Fgfr2NeoS252W, Fgfr2S252Wflox          Targeted (knock-in)       cardiovascular, cellular, craniofacial, digestive/alimentary, growth/size, hematopoietic, homeostasis, immune, mortality/aging, muscle, nervous system, respiratory, skeleton, vision/eye                                                          Apert Syndrome 101200                              

Fgfr2tm1Schl
fibroblast growth factor receptor 2; targeted mutation 1, Joseph Schlessinger
  7    Fgfr2cC342Y                            Targeted (knock-in)       craniofacial, digestive/alimentary, mortality/aging, respiratory, skeleton, vision/eye                                                                                                                                                             Crouzon Syndrome 123500                            

Fgfr2tm2.3Dsn
fibroblast growth factor receptor 2; targeted mutation 2.3, Clive Dickson
     7    Fgfr2delta, FgfR2-IIIcdelta            Targeted (knock-out)      craniofacial, digestive/alimentary, endocrine/exocrine, growth/size, homeostasis, liver/biliary, mortality/aging, renal/urinary, respiratory, skeleton, vision/eye                                                                                 Apert Syndrome 101200; Pfeiffer Syndrome 101600    

Fgfr2tm2Cxd
fibroblast growth factor receptor 2; targeted mutation 2, Chu-Xia Deng          7    Fgfr2neo250                            Targeted (Floxed/Frt)     craniofacial, embryogenesis, growth/size, mortality/aging, reproductive, skeleton, vision/eye                                                                                                                                                      Apert Syndrome 101200                              

Fgfr2tm2Ewj
fibroblast growth factor receptor 2; targeted mutation 2, Ethylin Wang Jabs     7    Fgfr2P253Rneo                          Targeted (knock-in)       cellular, craniofacial, digestive/alimentary, growth/size, limbs/digits/tail, mortality/aging, nervous system, skeleton, vision/eye                                                                                                                Apert Syndrome 101200                              

Fgfr2tm3Ewj
fibroblast growth factor receptor 2; targeted mutation 3, Ethylin Wang Jabs     7    Fgfr2Y394C                             Targeted (knock-in)       craniofacial, embryogenesis, growth/size, integument, mortality/aging, skeleton                                                                                                                                                                    Beare-Stevenson Cutis Gyrata Syndrome; BSTVS 123790

Fgfr2tm4Lni
fibroblast growth factor receptor 2; targeted mutation 4, Peter Lonai
           7    Fgfr2cC342Y                            Targeted (knock-in)       craniofacial, digestive/alimentary, mortality/aging, respiratory, skeleton, vision/eye                                                                                                                                                             Crouzon Syndrome 123500