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B6.C-H2-Kbm1/ByJ Strain Detail
Summary
  • Strain Name
    B6.C-H2-Kbm1/ByJ
  • Attributes
    chemically induced mutation, congenic, major histocompatibility congenic
  • MGI ID
    MGI:2163437
  • Synonyms
    B6.C-H2bm1/ByJ, HZ1
  • Other IDs
    JAX:001060
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
H2-Kbm1 H2-K
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
Usher syndrome type 1D
Key disease model expected model not found
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:001060 JAX B6.C-H2-Kbm1/ByJ exact match to ID
References
  • Earliest
    J:109263 Pease LR, et al., Spontaneous H-2 mutants provide evidence that a copy mechanism analogous to gene conversion generates polymorphism in the major histocompatibility complex. Proc Natl Acad Sci U S A. 1983 Jan;80(1):242-6
  • 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
04/09/2024
MGI 6.23
The Jackson Laboratory