| Human Disease |
Neuropathy, Hereditary Sensory and Autonomic, Type III; HSAN3 OMIM ID: 223900 |
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| Synonyms | Dysautonomia, Familial; DYS; FD; HSAN III; Riley-Day Syndrome | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Ikbkaptm1Id/Ikbkaptm1Id Tg(Hsp70-1-cre)6Arge/0 |
involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA | J:188923 | View |
| Ikbkaptm1Id/Ikbkaptm1.1Id Tg(Hsp70-1-cre)6Arge/0 |
involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA | J:188923 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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