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Symbol
Name
ID
Dctn1
dynactin 1
MGI:107745
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Weakness of facial musculature
Hand muscle atrophy
Hand muscle weakness
Lower limb muscle weakness
Rigidity
Spasticity
Muscle spasm
Muscle weakness
Distal muscle weakness
Skeletal muscle atrophy
Distal amyotrophy
Disease(s) Associated with DCTN1
amyotrophic lateral sclerosis type 1
autosomal dominant distal hereditary motor neuronopathy 14
Perry syndrome

Mouse Phenotypes
decreased gastrocnemius weight
skeletal muscle atrophy
Availability Mouse Genotype
Dctn1tm2.1Cai/Dctn1tm2.1Cai
Tg(Thy1-cre)1Vln/?  (conditional)

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)
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Funding Information
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory