| Human Disease |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 4; MDDGA4 OMIM ID: 253800 |
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| Synonyms | Fukuyama Congenital Muscular Dystrophy; FCMD; Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, Fktn-Related | |||||||||||||||||||||
| View all models | View ALL (5) 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 |
| Fktntm1Ttd/Fktntm1Ttd |
involves: 129S7/SvEvBrd * C57BL/6 | J:97950 | View |
| Fktntm1Ttd/Fktntm2(FCMD)Ttd |
involves: 129S7/SvEvBrd | J:144746 | View |
| Fktntm1.1Kcam/Fktntm1.1Kcam Myf5tm3(cre)Sor/Myf5+ |
involves: 129S/SvEv * 129S4/SvJaeSor | J:187144 | View |
| Fktntm1.1Kcam/Fktntm1.1Kcam Tg(Ckmm-cre)5Khn/? |
involves: 129S/SvEv * FVB | J:187144 | View |
| Fktntm1.1Kcam/Fktntm1.1Kcam Tg(CAG-cre/Esr1*)5Amc/? |
involves: 129S/SvEv * C57BL/6 * CBA | J:187144 | 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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