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C3H/HeJ-Lpin1fld-2J/J Strain Detail
Summary
  • Strain Name
    C3H/HeJ-Lpin1fld-2J/J
  • Attributes
    mutant strain, spontaneous mutation
  • MGI ID
    MGI:2164379
  • Synonyms
    nm2119
  • Other IDs
    JAX:003401
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Lpin1fld-2J Lpin1
Associated
Phenotypes
and
Diseases
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
normal phenotype
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
Human Diseases

model 1
lipodystrophy
Key disease model expected model not found
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:003401 JAX C3H/HeJ-Lpin1fld-2J/J exact match to ID
References
  • Earliest
    J:9801 Langner CA, et al., The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities. J Biol Chem. 1989 May 15;264(14):7994-8003
  • All

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
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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory