Excel File
Text File
All mouse models of autosomal dominant intellectual developmental disorder with phenotypic similarity to the human disease
|
||||||||
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 | ||||
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 |