DCTN1

dynactin subunit 1
OMIM: 601143
PanelMode of inheritanceDetails
3 panels
R-numbers: R56
Signed-off version 1.121
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Perry syndrome, OMIM:168605, Neuronopathy, distal hereditary motor, type VIIB, OMIM:607641
R-numbers: R78
Signed-off version 1.36
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Perry syndrome, 168605, {Amyotrophic lateral sclerosis, susceptibility to}, 105400, Neuropathy, distal hereditary motor, type VIIB 607641
R-numbers: R58
Signed-off version 2.178
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Neuropathy, distal hereditary motor, type VIIB, OMIM:607641, Perry syndrome, OMIM:168605, {Amyotrophic lateral sclerosis, susceptibility to}, OMIM:105400