| Human Disease |
Barth Syndrome; BTHS OMIM ID: 302060 |
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| Synonyms | 3-methylglutaconic Aciduria, Type II; MGCA2; Cardioskeletal Myopathy with Neutropenia and Abnormal Mitochondria; Mga, Type II; MGA2 | ||||||||||||||||||||||||||||||||
| 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 |
| Fkbp1atm1Zuk/Fkbp1atm1Zuk |
either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J) | J:45536 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Mesttm1Masu/Mest+ |
Not Specified | J:79223 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Gt(ROSA)26Sortm37(H1/tetO-RNAi:Taz)Arte/? |
Not Specified | J:176041 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Gt(ROSA)26Sortm37(H1/tetO-RNAi:Taz)Arte/Gt(ROSA)26Sor+ |
involves: 129S6/SvEvTac * C57BL/6J | J:167527 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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