| Human Disease |
Lecithin:cholesterol Acyltransferase Deficiency OMIM ID: 245900 |
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| Synonyms | LCAT Deficiency; Norum Disease | |||||||||||||||||||||
| 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 |
| Lcattm1Nsa/Lcattm1Nsa |
involves: 129X1/SvJ * C57BL/6J | J:39237 | View |
| Lcattm1Nsa/Lcat+ |
involves: 129X1/SvJ * C57BL/6J | J:39237 | 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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