| Human Disease |
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to OMIM ID: 311250 |
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| Synonyms | Ornithine Carbamoyltransferase Deficiency | |||||||||||||||||||||
| View all models | View ALL (7) 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 |
| Otcspf/Otcspf |
involves: CD-1 | J:784 | View |
| Otcspf-ash/Y |
B6EiC3Sn a/A-Otcspf-ash/J | J:108979 | View |
| Otcspf/Y |
involves: C3H/HeJ * C57BL/6J | J:31237 | View |
| Otcspf-ash/Y |
Not Specified | J:26977 | View |
| Otcspf/Y |
involves: C57BL/6 | J:1966 | View |
| Otcspf/Y |
involves: CD-1 | J:784, J:19848, J:23195 | View |
| Otcspf/Y |
Not Specified | J:7789, J:23017 | 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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