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Symbol Name ID |
Lipa
lysosomal acid lipase A MGI:96789 |
| Darker colors indicate more annotations |
| Human Phenotypes | Anemia |
Leukopenia |
Vacuolated lymphocytes |
Bone-marrow foam cells |
Disseminated intravascular coagulation |
Thrombocytopenia |
Splenomegaly |
Hepatosplenomegaly |
Hypersplenism |
| Disease(s) Associated with LIPA | |||||||||
| cholesterol ester storage disease | |||||||||
| lysosomal acid lipase deficiency | |||||||||
| Wolman disease |
| Mouse Phenotypes | abnormal Kupffer cell morphology |
hepatosplenomegaly |
enlarged spleen |
increased spleen weight |
abnormal alveolar macrophage morphology |
abnormal spleen morphology |
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| Availability | Mouse Genotype | ||||||
| Lipatm1Ggb/Lipatm1Ggb | |||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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