Excel File Text File All mouse models of craniosynostosis with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      craniosynostosis Tg(CMV-Msx2*P7H)1Rem/0 involves: C57BL/6 * CBA/J J:26513 View
craniosynostosis Tg(Msx2)1Rem/0 involves: C57BL/6 * CBA/J J:26513 View
craniosynostosis Tg(Timp1-Msx2*P7H)1Rem/0 involves: C57BL/6 * CBA/J J:26513 View
Crouzon syndrome Fgfr2m1Sgg/Fgfr2+ involves: C3H/HeJ * C57BL/6J J:160674 View
Crouzon syndrome Fgfr2m1Sgg/Fgfr2m1Sgg involves: C3H/HeJ * C57BL/6J J:160674 View
Crouzon syndrome Fgfr2tm1Schl/Fgfr2+ involves: 129S1/Sv J:118299 View
Crouzon syndrome Fgfr2tm4Lni/Fgfr2+ Not Specified J:92433, J:235329 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3+ 129S6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3+ B6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3+ CBACa.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw 129S6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw B6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw CBACa.129P2-Fgfr3tm1.1Aomw J:144356 View
      craniosynostosis Axin2tm1Wbm/Axin2tm1Wbm involves: 129P2/OlaHsd * C57BL/6 J:98523 View
Crouzon syndrome Bey/Bey+ 129S/SvEv-Bey J:47965 View
Transgenes and
Other Mutations		     craniosynostosis Tg(Nell1)1Ting/0 involves: C3H * C57BL/6 J:79106 View