Symbol Name ID |
Lipa
lysosomal acid lipase A MGI:96789 |
Darker colors indicate more annotations |
Human Phenotypes | Hepatic steatosis |
Portal hypertension |
Hepatosplenomegaly |
Hepatomegaly |
Increased hepatic echogenicity |
Cirrhosis |
Hepatic fibrosis |
Hepatic bridging fibrosis |
Periportal fibrosis |
Jaundice |
Disease(s) Associated with LIPA | ||||||||||
cholesterol ester storage disease | ||||||||||
Wolman disease |
Mouse Phenotypes | abnormal liver sinusoid morphology |
abnormal Kupffer cell morphology |
enlarged liver |
hepatosplenomegaly |
increased liver weight |
increased liver cholesterol level |
decreased liver triglyceride level |
increased liver triglyceride level |
liver inflammation |
abnormal liver morphology |
abnormal hepatocyte morphology |
hepatic steatosis |
liver fibrosis |
pale liver |
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Availability | Mouse Genotype | ||||||||||||||
Lipatm1Ggb/Lipatm1Ggb | |||||||||||||||
Lipatm1c(EUCOMM)Hmgu/Lipatm1c(EUCOMM)Hmgu Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1Tg(Alb-cre)21Mgn (conditional) |
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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