| Human Disease |
Ehlers-Danlos Syndrome, Type I OMIM ID: 130000 |
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| Synonyms | Eds I; EDS1; Ehlers-Danlos Syndrome, Gravis Type; Ehlers-Danlos Syndrome, Severe Classic Type | |||||||||||||||||||||||||||||||||||||||
| 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 |
| Col5a1tm1Rjw/Col5a1+ |
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) | J:113133 | View |
| Col5a1tm1Rjw/Col5a1+ |
involves: 129S6/SvEvTac * C57BL/6 | J:112728 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Lumtm1Chak/Lumtm1Chak |
involves: CD-1 | J:48068 | View |
| Fmodtm1Aol/Fmodtm1Aol Lumtm1Chak/Lumtm1Chak |
involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:79115 | 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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