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BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpefat/LtJng Strain Detail
Summary
  • Strain Name
    BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpefat/LtJng
  • Attributes
    congenic, spontaneous mutation, transgenic
  • MGI ID
    MGI:3785629
  • Synonyms
    BKSChpLt(HRS)-Tg(Ins2-Cpe)1Lt Cpefat/LtJng
Associated
Mutations,
Markers,
and QTL
2 associated mutations
Associated
Phenotypes
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.
References
  • Earliest
    J:134371 Kano K, et al., A novel dwarfism with gonadal dysfunction due to loss-of-function allele of the collagen receptor gene, Ddr2, in the mouse. Mol Endocrinol. 2008 Aug;22(8):1866-80
  • All
    12
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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory