About   Help   FAQ
B6.D2-Scn8amed-jo/J Strain Detail
Summary
  • Strain Name
    B6.D2-Scn8amed-jo/J
  • Attributes
    congenic, mutant strain, spontaneous mutation
  • MGI ID
    MGI:2165165
  • Synonyms
    C57BL/6J-Scn8amed-jo/J, jolting
  • Other IDs
    JAX:003799
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Scn8amed-jo Scn8a
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.
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:003799 JAX B6.D2-Scn8amed-jo/J exact match to ID
References
  • Earliest
    J:35567 Kohrman DC, et al., A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting. J Neurosci. 1996 Oct 1;16(19):5993-9
  • All
    1
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
10/29/2024
MGI 6.24 		The Jackson Laboratory