Symbol Name ID |
Dctn1
dynactin 1 MGI:107745 |
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 |
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Availability | Mouse Genotype | ||
Dctn1tm2.1Cai/Dctn1tm2.1Cai Tg(Thy1-cre)1Vln/? (conditional) |
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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last database update 04/09/2024 MGI 6.23 |
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