| Human Disease |
Erythrokeratodermia Variabilis Et Progressiva; EKVP OMIM ID: 133200 |
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| Synonyms | Erythrokeratodermia Figurata, Congenital Familial, in Plaques; Erythrokeratodermia Variabilis; EKV; Erythrokeratodermia, Progressive Symmetric; PSEK | ||||||||||||||||||||||||||||
| View all models | View ALL (1) 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 |
| Gjb3tm2.1Kwi/Gjb3+ |
involves: 129P2/OlaHsd * C57BL/6 | J:121802 | 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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