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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
![]() ![]() | autosomal dominant intellectual developmental disorder 7 | \Dyrk1aem1Kzy/\Dyrk1a+ | C57BL/6J-Dyrk1aem1Kzy | J:259596 | View | |||
autosomal dominant intellectual developmental disorder 26 | \Auts2tm1Mhos/\Auts2+ | C57BL/6N-Auts2tm1Mhos | J:261355 | View | ||||
autosomal dominant intellectual developmental disorder 38 | \Eef1a2em#Abb/\Eef1a2+ | C57BL/6JCrl-Eef1a2em#Abb | J:296080 | View | ||||
autosomal dominant intellectual developmental disorder 39 | \Myt1lem1Jdd/\Myt1l+ | C57BL/6-Myt1lem1Jdd/J | J:321206 | View | ||||
autosomal dominant intellectual developmental disorder 39 | \Myt1lem1Mwer/\Myt1l+ | involves: C57BL/6N | J:326588 | View | ||||
Coffin-Siris syndrome 1 | \Arid1bem1Hzhu/\Arid1b+ | C57BL/6J-Arid1bem1Hzhu | J:256668 | View | ||||
GAND syndrome | \Gatad2btm1a(EUCOMM)Hmgu/\Gatad2b+ | C57BL/6N-Gatad2btm1a(EUCOMM)Hmgu | J:344365 | View | ||||
Helsmoortel-Van Der Aa Syndrome | \Adnpem1Ant/\Adnp+ | Not Specified | J:101977 | View | ||||
Helsmoortel-Van Der Aa Syndrome | \Adnpem1Goz/\Adnp+ | C57BL/6N-Adnpem1Goz | J:361953 | View | ||||
neurodevelopmental disorder with dysmorphic facies and distal limb anomalies |
\Bptftm1.1Cwu/\Bptftm1.1Cwu \Emx1tm1(cre)Krj/\Emx1+ |
involves: 129S1/Sv * 129S2/SvPas * C57BL/6 | J:334252 | View | ||||
Pierpont syndrome | \Tbl1xr1em2H/\Tbl1xr1em2H | C57BL/6J-Tbl1xr1em2H | J:335355 | View | ||||
Xia-Gibbs Syndrome | \Ahdc1em#Oro/? | mosaic involves: C57BL/6 * CD-1 | J:326009 | View | ||||
![]() | autosomal dominant intellectual developmental disorder |
\Auts2tm1.1Dare/\Auts2tm1.1Dare \Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * SJL | J:217675 | View | |||
autosomal dominant intellectual developmental disorder | \Mbd5Gt(Ayu21-B205)Imeg/\Mbd5+ | B6.Cg-Mbd5Gt(Ayu21-B205)Imeg | J:212073 | View | ||||
autosomal dominant intellectual developmental disorder |
\Zbtb18tm1.1Nda/\Zbtb18tm1.1Nda \Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * SJL | J:184434 | View | ||||
Coffin-Siris syndrome |
\Arid1atm1.1Mag/\Arid1a+ \H2az2Tg(Wnt1-cre)11Rth/\H2az2+ |
involves: C57BL/6J * CBA/J | J:231470 | View | ||||
Coffin-Siris syndrome |
\Arid1atm1.1Mag/\Arid1atm1.1Mag \H2az2Tg(Wnt1-cre)11Rth/\H2az2+ |
involves: C57BL/6J * CBA/J | J:231470 | View |