Symbol Name ID |
Lcat
lecithin cholesterol acyltransferase MGI:96755 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Decreased HDL cholesterol concentration |
Hypertriglyceridemia |
Decreased lecithin cholesterol acyl transferase level |
Proteinuria |
Disease(s) Associated with LCAT | ||||
Norum disease |
Mouse Phenotypes | homeostasis/metabolism phenotype |
decreased circulating HDL cholesterol level |
increased circulating HDL cholesterol level |
decreased circulating VLDL cholesterol level |
decreased circulating cholesterol level |
increased circulating cholesterol level |
abnormal circulating phospholipid level |
increased circulating phospholipid level |
increased circulating triglyceride level |
abnormal circulating protein level |
abnormal lipid homeostasis |
abnormal cholesterol homeostasis |
decreased cholesterol level |
increased cholesterol level |
abnormal lipid level |
increased urine protein level |
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Availability | Mouse Genotype | ||||||||||||||||
Lcattm1Hgc/Lcattm1Hgc | |||||||||||||||||
Lcattm1Nsa/Lcattm1Nsa | * | ||||||||||||||||
Tg(Lcat)1Ssf/Tg(Lcat)1Ssf | |||||||||||||||||
Lcattm1Hgc/Lcat+ | |||||||||||||||||
Lcattm1Nsa/Lcat+ |
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 05/14/2024 MGI 6.23 |
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