| Human Disease |
Cutis Laxa, Autosomal Recessive, Type IA; ARCL1A OMIM ID: 219100 |
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| Synonyms | Arcl1; Cutis Laxa, Autosomal Recessive | |||||||||||||||||||||
| 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 |
| Fbln5tm1Krc/Fbln5tm1Krc |
involves: 129X1/SvJ * C57BL/6 | J:86753 | View |
| Fbln5tm1Eno/Fbln5tm1Eno |
involves: 129S6/SvEvTac | J:86754 | 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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