| Human Disease |
Pachyonychia Congenita, Type 2; PC2 OMIM ID: 167210 |
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| Synonyms | Pachyonychia Congenita, Jackson-Lawler Type | |||||||||||||||||||||||||
| 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 |
| Krt17tm1Cou/Krt17tm1Cou Krt6a/Krt6btm1Cou/Krt6a/Krt6btm1Cou Krt6a/Krt6btm1Cou/Krt6a/Krt6btm1Cou |
involves: 129S2/SvPas * C57BL/6 | J:95390 | 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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