About   Help   FAQ
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
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory