About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:8401702
Allelic
Composition
Nek1em1Hdt/Nek1+
Pmlem10Hdt/Pmlem10Hdt
Genetic
Background
FVB/N-Nek1em1Hdt Pmlem10Hdt
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nek1em1Hdt mutation (0 available); any Nek1 mutation (84 available)
Pmlem10Hdt mutation (0 available); any Pml mutation (94 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• shortened lifespan, partial penetrance

growth/size/body
• mice show significant weight loss beginning at 60-70 weeks of age

nervous system
• mice exhibit amyotrophic lateral sclerosis-like phenotypes, with mean onset of neurological symptoms at 31.5 weeks

behavior/neurological
• impaired coordination and motor function starting at 31.5 weeks after birth on the hanging wire
• grip strength and limb clasping show an age-dependent, progressive decline in muscle strength and motor function

muscle
• severe muscle weakness

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
amyotrophic lateral sclerosis type 24 DOID:0081378 OMIM:617892
J:390648


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
07/14/2026
MGI 6.24
The Jackson Laboratory