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BALB/cJ-Enpp1asj-2J/GrsrJ Strain Detail
Summary
  • Strain Name
    BALB/cJ-Enpp1asj-2J/GrsrJ
  • Attributes
    coisogenic, mutant strain, spontaneous mutation
  • MGI ID
    MGI:5607166
  • Other IDs
    JAX:019107
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Enpp1asj-2J Enpp1
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
arterial calcification of infancy
Key disease model expected model not found
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:019107 JAX BALB/cJ-Enpp1asj-2J/GrsrJ exact match to ID
References
  • Earliest
    J:215824 Li Q, et al., Spontaneous asj-2J mutant mouse as a model for generalized arterial calcification of infancy: a large deletion/insertion mutation in the Enpp1 gene. PLoS One. 2014;9(12):e113542
  • 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
02/11/2020
MGI 6.14
The Jackson Laboratory