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B6.Cg-Pmp22Tr-J Krt25Re/+ +/J Strain Detail
Summary
  • Strain Name
    B6.Cg-Pmp22Tr-J Krt25Re/+ +/J
  • Attributes
    congenic, mutant strain
  • MGI ID
    MGI:2161321
  • Synonyms
    B6.Cg-Pmp22Tr-J Re/+ +/J
  • Other IDs
    JAX:000568
Associated
Mutations,
Markers,
and QTL
2 associated mutations
Mutation Carried Marker
Krt25Re Krt25
Pmp22Tr-J Pmp22
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
Charcot-Marie-Tooth disease type 1A
Key disease model expected model not found
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:000568 JAX B6.Cg-Pmp22Tr-J Krt25Re/+ +/J exact match to ID
References
  • Earliest
    J:7222 Henry EW, et al., Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination. J Neuropathol Exp Neurol. 1983 Nov;42(6):688-706
  • 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
11/12/2024
MGI 6.24
The Jackson Laboratory