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All mouse models of syndromic intellectual disability with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
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 | ||||
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 midbrain and hindbrain malformations | Arhgef2Gt(IST13976A8)Tigm/Arhgef2Gt(IST13976A8)Tigm | involves: C57BL/6N | J:242973 | View | ||||
Renpenning syndrome |
Pqbp1tm1.1Hiok/Y Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * C57BL/6J | J:279053 | 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 | ||||
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 |