About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/07/2024
MGI 6.23
The Jackson Laboratory