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All mouse models of intellectual disability with phenotypic similarity to the human disease
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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 | ||||
autosomal recessive intellectual developmental disorder 41 | Kptntm1a(EUCOMM)Wtsi/Kptntm1a(EUCOMM)Wtsi | C57BL/6N-Kptntm1a(EUCOMM)Wtsi | J:343200 | View | ||||
Borjeson-Forssman-Lehmann syndrome | Phf6em1Azbi/Y | B6.Cg-Phf6em1Azbi | J:271089 | View | ||||
Borjeson-Forssman-Lehmann syndrome | Phf6tm1.2Avo/Y | involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N | J:299742 | View | ||||
Christianson syndrome | Slc9a6tm1Dgen/Slc9a6+ | B6.129P2-Slc9a6tm1Dgen/J | J:229166 | View | ||||
Christianson syndrome | Slc9a6tm1Dgen/Slc9a6tm1Dgen | B6.129P2-Slc9a6tm1Dgen/J | J:241124 | View | ||||
Christianson syndrome | Slc9a6tm1Dgen/Y | B6.129P2-Slc9a6tm1Dgen/J | J:241124, J:229166, J:262453 | 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 | ||||
Kaufman oculocerebrofacial syndrome | Ube3btm1a(EUCOMM)Hmgu/Ube3btm1a(EUCOMM)Hmgu | C57BL/6-Ube3btm1a(EUCOMM)Hmgu | J:273879 | View | ||||
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations | Mast1em1Dak/Mast1+ | B6.Cg-Mast1em1Dak | J:268904 | 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 | ||||
neurodevelopmental disorder with midbrain and hindbrain malformations | Arhgef2Gt(IST13976A8)Tigm/Arhgef2Gt(IST13976A8)Tigm | involves: C57BL/6N | J:242973 | View | ||||
non-syndromic X-linked intellectual developmental disorder 111 |
Slitrk2tm1.1Jwum/Y Tg(Nes-cre)1Atp/0 |
involves: C57BL/6J * FVB/N | J:342291 | View | ||||
non-syndromic X-linked intellectual disability | Gdi1tm1Toni/Y | B6N.129S7-Gdi1tm1Toni | J:142806 | View | ||||
non-syndromic X-linked intellectual disability 9 | Ftsj1tm1Tomik/Y | Not Specified | J:328916 | View | ||||
non-syndromic X-linked intellectual disability 30 | Pak3tm1.1Rpo/Y | B6.129S2(Cg)-Pak3tm1.1Rpo | J:292116 | View | ||||
non-syndromic X-linked intellectual disability 72 | Rab39btm1Pdad/Y | B6N.Cg-Rab39btm1Pdad | J:341888 | View | ||||
non-syndromic X-linked intellectual disability 98 | Nexmiftm1(KOMP)Wtsi/Y | B6J.B6N-Nexmiftm1(KOMP)Wtsi | J:283395 | View | ||||
Pierpont syndrome | Tbl1xr1em2H/Tbl1xr1em2H | C57BL/6J-Tbl1xr1em2H | J:335355 | View | ||||
Renpenning syndrome |
Pqbp1tm1.1Hiok/Y Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * C57BL/6J | J:279053 | View | ||||
spastic tetraplegia, thin corpus callosum, and progressive microcephaly | Slc1a4em2Tmg/Slc1a4em2Tmg | involves: C57BL/6J | J:344184 | View | ||||
syndromic X-linked intellectual developmental disorder bain type | Hnrnph2em1Jpat/Hnrnph2+ | C57BL/6J-Hnrnph2em1Jpat | J:338313 | View | ||||
syndromic X-linked intellectual developmental disorder bain type | Hnrnph2em1Jpat/Y | C57BL/6J-Hnrnph2em1Jpat | J:338313 | View | ||||
syndromic X-linked intellectual developmental disorder bain type | Hnrnph2em2Jpat/Y | C57BL/6J-Hnrnph2em2Jpat | J:338313 | View | ||||
syndromic X-linked intellectual disability 5 | Ap1s2tm1Pschu/Ap1s2tm1Pschu | involves: 129P2/OlaHsd * C57BL/6 | J:218588 | View | ||||
syndromic X-linked intellectual disability Claes-Jensen type | Kdm5ctm1.2Yshi/Y | involves: 129 * 129S1/SvImJ * C57BL/6J | J:262206 | View | ||||
syndromic X-linked intellectual disability Raymond type | Zdhhc9tm1Lex/Y | B6.129S5-Zdhhc9tm1Lex | J:268248 | View | ||||
syndromic X-linked intellectual disability Siderius type | Phf8tm1.1Cdcn/Y | B6.129S6(Cg)-Phf8tm1.1Cdcn | J:258245 | View | ||||
X-linked intellectual disability-short stature-overweight syndrome | Thoc2em1Gecz/Y | C57BL/6JArc-Thoc2em1Gecz | J:345229 | 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 | ||||
autosomal recessive intellectual developmental disorder |
Crbntm1.1Jjh/Crbntm1.1Jjh Tg(Camk2a-cre)T29-1Stl/0 |
involves: C57BL/6 | J:179427 | View | ||||
autosomal recessive intellectual developmental disorder | Crbntm1.2Jjh/Crbntm1.2Jjh | involves: C57BL/6 | J:259276 | 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 | ||||
intellectual disability |
Cul4btm1Swl/Y Edil3Tg(Sox2-cre)1Amc/Edil3+ |
B6.Cg-Edil3Tg(Sox2-cre)1Amc Cul4btm1Swl | J:187403 | View | ||||
intellectual disability | Elp2em2Bjw/Elp2em2Bjw | involves: C57BL/6 | J:306113 | View | ||||
intellectual disability | Elp2em2Bjw/Elp2em2Bjw | involves: C57BL/6 * DBA/2J | J:306113 | View | ||||
intellectual disability | Elp2em2Bjw/Elp2em3Bjw | involves: C57BL/6 * DBA/2J | J:306113 | View | ||||
intellectual disability | Fgf13em1Xuzh/Y | involves: C57BL/6J | J:307501 | View | ||||
intellectual disability | Gprasp2tm1.1Jpe/Y | B6.129(FVB)-Gprasp2tm1.1Jpe | J:273373 | View | ||||
intellectual disability | Hivep2tm1Sis/Hivep2tm1Sis | involves: C57BL/6NCrlj * CBA/JNCrlj | J:271912 | View | ||||
intellectual disability | Trappc9em1Xyli/Trappc9em1Xyli | C57BL/6J-Trappc9em1Xyli | J:304877 | View | ||||
intellectual disability | Trappc9tm1a(EUCOMM)Wtsi/Trappc9tm1a(EUCOMM)Wtsi | involves: C57BL/6N | J:294716 | View | ||||
non-syndromic X-linked intellectual disability | Dlg3tm1Grnt/Y | involves: 129P2/OlaHsd * C57BL/6J | J:238576 | View | ||||
non-syndromic X-linked intellectual disability | Iqsec2em1Csbg/Y | C57BL/6NHsd-Iqsec2em1Csbg | J:284750 | View | ||||
non-syndromic X-linked intellectual disability | Iqsec2em1Frk/Y | involves: C3HeB/FeJ * C57BL/6NJ | J:284762 | View | ||||
syndromic intellectual disability | Anapc7tm1.1Azbi/Anapc7tm1.1Azbi | B6.129S6(CBA)-Anapc7tm1.1Azbi | J:320745 | View | ||||
syndromic intellectual disability |
Brpf1tm1c(EUCOMM)Wtsi/Brpf1tm1c(EUCOMM)Wtsi Emx1tm1(cre)Krj/Emx1+ |
involves: 129S2/SvPas * C57BL/6J * C57BL/6N | J:240552 | View | ||||
syndromic intellectual disability | Brpf1tm1d(EUCOMM)Wtsi/Brpf1tm1d(EUCOMM)Wtsi | involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N | J:240552 | View | ||||
syndromic intellectual disability | Ophn1tm1Bill/Y | involves: 129S2/SvPas | J:124943 | View | ||||
syndromic X-linked intellectual disability | Arxtm1.1Ics/Y | involves: 129S2/SvPas * C57BL/6J * C57BL/6N | J:262482 | View | ||||
syndromic X-linked intellectual disability | Rab39bem1Jfch/Y | C57BL/6N-Rab39bem1Jfch | J:287752 | View | ||||
syndromic X-linked intellectual disability Lubs type | Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae | B6.Cg-Mapttm1(Mecp2)Jae | J:182685 | View | ||||
Transgenes and Other Mutations | syndromic intellectual disability | Del(17Abcg1-Rrp1b)5Yey/+ | 129S.129S7-Del(17Abcg1-Rrp1b)5Yey | J:161398 | View | |||
syndromic X-linked intellectual disability Lubs type | Tg(MECP2)1Hzo/0 | either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1 | J:181213 | View | ||||
syndromic X-linked intellectual disability Lubs type | Tg(MECP2)1Hzo/0 | FVB-Tg(MECP2)1Hzo/J | J:253720 | View | ||||
syndromic X-linked intellectual disability Lubs type | Tg(MECP2)3Hzo/0 | either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1 | J:181213 | View |