![]() ![]() |
||||||||
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 |
No similarity to the expected human disease phenotype was found.
|
||||||||
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 |