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Symbol
Name
ID
Lpl
lipoprotein lipase
MGI:96820
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Premature coronary artery atherosclerosis
Precocious atherosclerosis
Hypertension
Sudden cardiac death
Myocardial infarction
Splenomegaly
Hepatosplenomegaly
Lipemia retinalis
Disease(s) Associated with LPL
coronary artery disease
familial combined hyperlipidemia
familial lipoprotein lipase deficiency

Mouse Phenotypes
abnormal capillary morphology
liver vascular congestion
abnormal lung vasculature morphology
pulmonary vascular congestion
decreased cardiac muscle triglyceride level
cardiac fibrosis
cardiac interstitial fibrosis
abnormal cardiovascular system physiology
increased cardiac muscle cell glucose uptake
decreased cardiac muscle contractility
increased left ventricle diastolic pressure
increased left ventricle systolic pressure
Availability Mouse Genotype
Lpltm1Bres/Lpltm1Bres
Lpltm1Sem/Lpltm1Sem
Lpltm1Ijg/Lpltm1Ijg
Tg(Myh6-cre)2182Mds/?  (conditional)
Lpltm1Ijg/Lpltm1Ijg
Tg(Myh6-cre)2182Mds/0  (conditional)

Contributing Projects:
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
05/28/2024
MGI 6.13
The Jackson Laboratory