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All mouse models of dental enamel hypoplasia with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | amelogenesis imperfecta hypomaturation type 2A2 | Mmp20tm1Jdb/Mmp20tm1Jdb | involves: 129P2/OlaHsd * C57BL/6 | J:80925 | View | |||
| amelogenesis imperfecta hypomaturation type 2A3 | Wdr72tm1a(KOMP)Wtsi/Wdr72tm1a(KOMP)Wtsi | involves: C57BL/6N | J:215636 | View | ||||
| amelogenesis imperfecta type 1B | EnamRgsc395/Enam+ | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
| amelogenesis imperfecta type 1B | EnamRgsc514/Enam+ | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
| amelogenesis imperfecta type 1B | EnamRgsc521/Enam+ | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
| amelogenesis imperfecta type 1B | EnamRgsc521/EnamRgsc521 | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
| amelogenesis imperfecta type 1B | Enamtm1.1Jcch/Enam+ | involves: C57BL/6 | J:223123 | View | ||||
| amelogenesis imperfecta type 1B | Enamtm1.1Jcch/Enamtm1.1Jcch | involves: C57BL/6 | J:223123 | View | ||||
| amelogenesis imperfecta type 1E | AmelxRgsc888/Amelx+ | involves: C57BL/6JJcl * DBA/2J | J:157947 | View | ||||
| amelogenesis imperfecta type 1E | AmelxRgsc888/AmelxRgsc888 | involves: C57BL/6JJcl * DBA/2J | J:157947 | View | ||||
| amelogenesis imperfecta type 1E | AmelxRgsc888/Y | involves: C57BL/6JJcl * DBA/2J | J:157947 | View | ||||
| amelogenesis imperfecta type 1E | Amelxtm1Kul/Amelxtm1Kul | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:71126 | View | ||||
| amelogenesis imperfecta type 1E |
Amelxtm1Kul/Amelxtm1Kul Tg(AMELX*P70T)2Gibs/? |
involves: 129S1/Sv * 129X1/SvJ | J:122914 | View | ||||
| amelogenesis imperfecta type 1E | Tg(AMELX*P70T)2Gibs/? | Not Specified | J:122914 | View | ||||
| amelogenesis imperfecta type 3C | Reltem1Jpsi/Reltem1Jpsi | C57BL/6-Reltem1Jpsi | J:279949 | View | ||||
| Transgenes and Other Mutations | amelogenesis imperfecta | Tg(Amelx-Ambn)1Mlp/Tg(Amelx-Ambn)1Mlp | Not Specified | J:83576 | View | |||
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No similarity to the expected human disease phenotype was found.
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
| NOT Models | amelogenesis imperfecta type 1E | Tg(Amelx)42Msnd/Tg(Amelx)42Msnd | involves: C57BL/6J * CBA/J * DBA/2J | J:100004 | View | |||