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Adult onset dystonia, chorea or related movement disorder v1.42 DCTN1 Arina Puzriakova Phenotypes for gene: DCTN1 were changed from Perry syndrome to Perry syndrome, OMIM:168605; Neuronopathy, distal hereditary motor, type VIIB, OMIM:607641
Adult onset dystonia, chorea or related movement disorder v0.54 DCTN1 Louise Daugherty reviewed gene: DCTN1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.53 DCTN1 James Polke reviewed gene: DCTN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.52 DCTN1 Louise Daugherty Source NHS GMS was added to DCTN1.
Adult onset dystonia, chorea or related movement disorder v0.51 DCTN1 Louise Daugherty Source London North GLH was added to DCTN1.
Adult onset dystonia, chorea or related movement disorder v0.2 DCTN1 Ellen McDonagh gene: DCTN1 was added
gene: DCTN1 was added to Adult onset movement disorder. Sources: Expert Review Green
Mode of inheritance for gene: DCTN1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: DCTN1 were set to 20945553 (Gene Reviews); 24343258; 20437543; 19136952; 27132499; 27346608
Phenotypes for gene: DCTN1 were set to Perry syndrome