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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lipilpd1
lipid defect
MGI:2450247
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lipilpd1/Lipilpd1 involves: CD-1 MGI:3045800


Genotype
MGI:3045800
hm1
Allelic
Composition
Lipilpd1/Lipilpd1
Genetic
Background
involves: CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lipilpd1 mutation (0 available); any Lipi mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• death by 10 to 15 days of age

behavior/neurological
• generalized tremor developing 5 to 10 days after birth
• unsteady gait developing 5 to 10 days after birth

growth/size/body
• not a result from a failure to nurse, as milk was observed in the stomach
• exhibited ~3 days after birth

homeostasis/metabolism
• 2 to 3 fold increase in plasma triglyceride levels, whereas plasma cholesterol levels were normal
• increased hepatic triglyceride level, whereas hepatic cholesterol levels were normal

liver/biliary system
• increased hepatic triglyceride level, whereas hepatic cholesterol levels were normal
• numerous lipid-containing vacuoles with extensive triglyceride accumulation
• in severe cases, only ~20% of normal hepatic structure was left

integument





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
11/19/2024
MGI 6.24
The Jackson Laboratory