About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:5435676
Allelic
Composition
Fktntm1Kcam/Fktntm1Kcam
Myf5tm3(cre)Sor/Myf5+
Genetic
Background
involves: 129S/SvEv * 129S4/SvJaeSor
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fktntm1Kcam mutation (1 available); any Fktn mutation (12 available)
Myf5tm3(cre)Sor mutation (1 available); any Myf5 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 11% die before 20 weeks of age even with special feeding
• remainder are dead or euthanized by 35 weeks

growth/size/body
• significantly under weight
• combined gastrocnemius and soleus weight is low

muscle
• moderate to severe dystrophic features in the iliopsoas muscle at 20 weeks

homeostasis/metabolism
• elevated at 4 and 8 weeks

behavior/neurological
• forelimb grip strength is reduced

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Fukuyama congenital muscular dystrophy DOID:0050559 OMIM:253800
J:187144


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
05/16/2017
MGI 6.09
The Jackson Laboratory