| Human Disease |
Adenine Phosphoribosyltransferase Deficiency; APRTD OMIM ID: 614723 |
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| Synonyms | Aprt Deficiency; Nephrolithiasis, Dha; Urolithiasis, 2,8-dihydroxyadenine; Urolithiasis, Dha | |||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Aprttm1Jat/Aprttm1Jat |
involves: 129S2/SvPas * Black Swiss | J:33255 | View |
| Aprttm1Jat/Aprttm1Jat |
involves: 129S2/SvPas * C57BL/6J | J:33255 | View |
| Aprttm1Dwm/Aprttm1Dwm |
involves: 129P2/OlaHsd * BALB/c | J:38450 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/12/2013 MGI 5.14 |
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