| Human Disease |
Purine Nucleoside Phosphorylase Deficiency OMIM ID: 613179 |
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| Synonyms | Nucleoside Phosphorylase Deficiency | |||||||||||||||||||||
| View all models | View ALL (5) 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 |
| Pnpf/Pnpf |
C57BL/6J-Pnpf | J:39328 | View |
| Pnpg/Pnpg |
involves: C57BL/6 * DBA/2J | J:39328 | View |
| Pnpe/Pnpe |
C57BL/6J-Pnpe | J:39328 | View |
| Pnpe/Pnpe |
involves: C3H/HeHa * C57BL/6J | J:23354 | View |
| Pnpf/Pnpf |
involves: C3H/HeHa * C57BL/6J | J:23354 | 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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