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Symbol
Name
ID

Dctn1
dynactin 1
MGI:107745

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Pseudobulbar paralysis	Vocal cord paralysis	Depression	Apathy	Inappropriate behavior	Personality changes	Disinhibition	Hyperorality	Weak voice
Disease(s) Associated with DCTN1	Pseudobulbar paralysis	Vocal cord paralysis	Depression	Apathy	Inappropriate behavior	Personality changes	Disinhibition	Hyperorality	Weak voice
amyotrophic lateral sclerosis type 1
autosomal dominant distal hereditary motor neuronopathy 14
Perry syndrome

Mouse Phenotypes		limb grasping	impaired coordination	short stride length	decreased vertical activity
Availability	Mouse Genotype	limb grasping	impaired coordination	short stride length	decreased vertical activity
	Dctn1^tm1Cai/Dctn1⁺
	Dctn1^tm2.1Cai/Dctn1^tm2.1Cai 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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