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All mouse models of autosomal recessive intellectual developmental disorder with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
autosomal recessive intellectual developmental disorder 41 | Kptntm1a(EUCOMM)Wtsi/Kptntm1a(EUCOMM)Wtsi | C57BL/6N-Kptntm1a(EUCOMM)Wtsi | J:343200 | View | ||||
spastic tetraplegia, thin corpus callosum, and progressive microcephaly | Slc1a4em2Tmg/Slc1a4em2Tmg | involves: C57BL/6J | J:344184 | 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 |