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B10.D2-H2d/nSnJ Strain Detail
Summary
  • Strain Name
    B10.D2-H2d/nSnJ
  • Attributes
    congenic, major histocompatibility congenic, mutant strain
  • MGI ID
    MGI:2160632
  • Synonyms
    B10.D2-H2d/nSnJ (Non-Standard)
Associated
Mutations,
Markers,
and QTL
2 associated mutations
Mutation Carried Marker
H2
H2d H2
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
Griscelli syndrome type 1 √
Key √ disease model expected model not found
References
  • Earliest
    J:23983 Wetsel RA, et al., Deficiency of the murine fifth complement component (C5). A 2-base pair gene deletion in a 5'-exon. J Biol Chem. 1990 Feb 15;265(5):2435-40
  • All
    2
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
11/12/2024
MGI 6.24 		The Jackson Laboratory