| Human Disease |
Pelizaeus-Merzbacher Disease; PMD OMIM ID: 312080 |
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| Synonyms | Leukodystrophy, Hypomyelinating, 1; HLD1 | |||||||||||||||||||||
| View all models | View ALL (6) 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Plp1tm1Frca/Y |
B6.129-Plp1tm1Frca | J:143305 | View |
| Plp1jp-msd/Y |
involves: C3H * C57BL/6 * C57BL/10 * BALB/c | J:121540 | View |
| Plp1tm1Kan/? |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:146665 | View |
| Plp1jp-rsh/Y |
involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr | J:121540 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Plp)66Kan/Tg(Plp)66Kan |
B6NCrl.Cg-Tg(Plp)66Kan | J:156106 | View |
| Tg(Plp)66Kan/0 |
B6NCrl.Cg-Tg(Plp)66Kan | J:156106 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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