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All mouse models of craniosynostosis with phenotypic similarity to the human disease
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| 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 | |||