Excel File Text File All mouse models of intellectual disability 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
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
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
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
spastic tetraplegia, thin corpus callosum, and progressive microcephaly Slc1a4em2Tmg/Slc1a4em2Tmg involves: C57BL/6J J:344184 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 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 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