| Human Disease |
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of; ACADVLD OMIM ID: 201475 |
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| Synonyms | Vlcad Deficiency | ||||||||||||||||||||||||||||
| View all models | View ALL (4) 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 |
| Acadvltm1Uab/Acadvltm1Uab |
involves: 129S6/SvEvTac * C57BL/6 | J:72193 | View |
| Acadvltm1Vje/Acadvltm1Vje |
involves: 129/Sv * Black Swiss * C57BL/6 | J:106714 | View |
| Acadvltm1Vje/Acadvltm1Vje |
involves: 129/Sv * C57BL/6 | J:98627, J:102010 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Acadltm1Uab/Acadltm1Uab |
involves: 129S6/SvEvTac * C57BL/6NTac | J:51660 | 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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