| Human Disease |
Epidermolysis Bullosa, Junctional, Herlitz Type OMIM ID: 226700 |
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| Synonyms | Epidermolysis Bullosa Junctionalis, Herlitz Type; Epidermolysis Bullosa Letalis; Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type; Herlitz-Pearson-Type Epidermolysis Bullosa; Jeb-Herlitz Type | |||||||||||||||||||||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Lamc2tm1Uit/Lamc2tm1Uit |
involves: C57BL/6 | J:85981 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Itga6tm1Egl/Itga6tm1Egl |
either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129S2/SvPas * C57BL/6 * CD-1) | J:33712 | 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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