About   Help   FAQ
C57BL/6J-Nemftvrm116/PjnCx Strain Detail
Summary
  • Strain Name
    C57BL/6J-Nemftvrm116/PjnCx
  • Attributes
    chemically induced mutation, coisogenic, mutant strain
  • MGI ID
    MGI:6718875
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Nemftvrm116 Nemf
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
neuromuscular disease √
neuropathy √
Key √ disease model expected model not found
References
  • Earliest
    J:296528 Martin PB, et al., NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease. Nat Commun. 2020 Sep 15;11(1):4625
  • 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
11/12/2024
MGI 6.24 		The Jackson Laboratory