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B6.Cg-Fxntm1.1Pand Fxntm1Mkn/J Strain Detail
Summary
  • Strain Name
    B6.Cg-Fxntm1.1Pand Fxntm1Mkn/J
  • Attributes
    congenic, mutant strain, targeted mutation
  • MGI ID
    MGI:5426434
  • Other IDs
    JAX:012329
Associated
Mutations,
Markers,
and QTL
2 associated mutations
Mutation Carried Marker
Fxntm1.1Pand Fxn
Fxntm1Mkn Fxn
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
Friedreich ataxia
Key disease model expected model not found
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:012329 JAX B6.Cg-Fxntm1.1Pand Fxntm1Mkn/J exact match to ID
References
  • Earliest
    J:62185 Cossee M, et al., Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation. Hum Mol Genet. 2000 May 1;9(8):1219-26
  • 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
09/17/2019
MGI 6.14
The Jackson Laboratory