| Human Disease |
Citrullinemia, Type II, Neonatal-Onset OMIM ID: 605814 |
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| Synonyms | Cholestasis, Neonatal Intrahepatic, Caused By Citrin Deficiency; NICCD | |||||||||||||||||||||
| View all models | View ALL (1) 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 |
| Gpd2tm1Tka/Gpd2tm1Tka Slc25a13tm1Lct/Slc25a13tm1Lct |
B6.Cg-Gpd2tm1Tka Slc25a13tm1Lct | J:124766 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc25a13tm1Lct/Slc25a13tm1Lct |
either: 129/Sv-Slc25a13tm1Lct or (involves: 129S1/Sv * 129X1/SvJ * CD-1) | J:87578 | 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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