| Human Disease |
Dyskeratosis Congenita, X-Linked; DKCX OMIM ID: 305000 |
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| Synonyms | Zinsser-Cole-Engman Syndrome | |||||||||||||||||||||
| 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 |
| Dkc1tm1Ppp/Dkc1+ |
involves: 129S1/Sv | J:81054 | View |
| Dkc1tm1Ppp/Y |
involves: 129S1/Sv | J:81054 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Dkc1tm3Pjma/Dkc1tm3Pjma |
involves: 129X1/SvJ * C57BL/6J | J:149894 | View |
| Dkc1tm2Pjma/Y |
chimera involves: 129X1/SvJ * C57BL/6J | J:149894 | View |
| Dkc1tm3Pjma/Y |
involves: 129X1/SvJ * C57BL/6J | J:149894 | 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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