| Human Disease |
Rhizomelic Chondrodysplasia Punctata, Type 1; RCDP1 OMIM ID: 215100 |
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| Synonyms | Chondrodysplasia Punctata, Rhizomelic Form; CDPR; Chondrodystrophia Calcificans Punctata; Peroxisome Biogenesis Disorder 9; PBD9 | |||||||||||||||||||||
| 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 |
| Pex7tm1Rjaw/Pex7tm1Rjaw |
Swiss | J:92346 | View |
| Pex7tm1Nbra/Pex7tm1Nbra |
involves: 129S/SvEv * C57BL/6 | J:158845 | 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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