About   Help   FAQ
B6.129S4-Scn4atm1.1Ljh Strain Detail
Summary
  • Strain Name
    B6.129S4-Scn4atm1.1Ljh
  • Attributes
    congenic, mutant strain, targeted mutation
  • MGI ID
    MGI:4420407
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Scn4atm1.1Ljh Scn4a
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 model 2
hyperkalemic periodic paralysis √ √
Key √ disease model expected model not found
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
12/10/2024
MGI 6.24 		The Jackson Laboratory