| Human Disease |
Agenesis of the Corpus Callosum with Peripheral Neuropathy; ACCPN OMIM ID: 218000 |
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| Synonyms | Andermann Syndrome; Charlevoix Disease; Corpus Callosum, Agenesis of, with Neuronopathy; Polyneuropathy, Sensorimotor, with or without Agenesis of the Corpus Callosum | |||||||||||||||||||||
| View all models | View ALL (3) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc12a6tm1Dlp/Slc12a6tm1Dlp |
involves: 129 * C57BL/6J | J:79870 | View |
| Slc12a6tm1Tjj/Slc12a6tm1Tjj |
involves: 129/Sv * C57BL/6 | J:86183 | View |
| Slc12a6tm1Garo/Slc12a6tm1Garo Tg(Syn1-cre)671Jxm/0 |
involves: 129 * C57BL/6 * CBA | J:183239 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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