DCTN1 Chromosome 2

Dynactin subunit 1
82 variants 82 Health Risk

Upload your DNA to see your personal genotypes for variants in DCTN1.

What This Gene Does
This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. Dynactin is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit interacts with dynein intermediate chain by its domains directly binding to dynein and binds to microtubules via a highly conserved glycine-rich cytoskeleton-associated protein (CAP-Gly) domain in its N-terminus. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA). [provided by RefSeq, Oct 2008]
Gene Info
Gene Group
Dynactin subunits
Locus Type
gene with protein product
Location
2p13.1
Ensembl
ENSG00000204843
Associated Conditions (25)
Neuronopathy
distal hereditary motor
type 7B
Perry syndrome
Amyotrophic lateral sclerosis type 1
Inborn genetic diseases
Amyotrophic lateral sclerosis
susceptibility to
Charcot-Marie-Tooth disease
DCTN1-related disorder
Hereditary motor neuron disease
Frontotemporal dementia
Thymoma
Melanoma
Cholangiocarcinoma
Acute myeloid leukemia
Colorectal cancer
Ovarian serous cystadenocarcinoma
Malignant tumor of esophagus
Uterine corpus endometrial carcinoma
+5 more conditions
Key Variants
RS1032786897
Conflicting classifications of pathogenicity
Neuronopathy, distal hereditary motor, type 7B
Health Risk
RS1207333910
Conflicting classifications of pathogenicity
Inborn genetic diseases, Amyotrophic lateral sclerosis type 1, Perry syndrome
Health Risk
RS121909344
Conflicting classifications of pathogenicity
Amyotrophic lateral sclerosis, susceptibility to, Charcot-Marie-Tooth disease
Health Risk
RS1235693710
Conflicting classifications of pathogenicity
Neuronopathy, distal hereditary motor, type 7B
Health Risk
RS1299296008
Conflicting classifications of pathogenicity
Amyotrophic lateral sclerosis type 1, Neuronopathy, distal hereditary motor
Health Risk
RS1393363759
Conflicting classifications of pathogenicity
Neuronopathy, distal hereditary motor, type 7B
Health Risk
RS140066692
Conflicting classifications of pathogenicity
Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
Health Risk
RS142318791
Conflicting classifications of pathogenicity
Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
Health Risk
RS143914684
Conflicting classifications of pathogenicity
Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
Health Risk
RS145819459
Conflicting classifications of pathogenicity
Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
Health Risk
RS146083590
Conflicting classifications of pathogenicity
Neuronopathy, distal hereditary motor, type 7B
Health Risk
RS146896442
Conflicting classifications of pathogenicity
Inborn genetic diseases, Amyotrophic lateral sclerosis type 1, Perry syndrome
Health Risk
All Variants (82)
RSID Category Clinical Significance Conditions
RS758320436 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS758387062 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS759276455 Health Risk Conflicting classifications of pathogenicity Perry syndrome, Neuronopathy, distal hereditary motor
RS763226083 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Amyotrophic lateral sclerosis type 1, Perry syndrome
RS764443534 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS769145486 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS770153273 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS770872113 Health Risk Conflicting classifications of pathogenicity Perry syndrome, Amyotrophic lateral sclerosis type 1, Neuronopathy
RS771075973 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS771325809 Health Risk Conflicting classifications of pathogenicity Perry syndrome, Neuronopathy, distal hereditary motor
RS772608973 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Amyotrophic lateral sclerosis type 1, Neuronopathy
RS776489779 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS778201974 Health Risk Conflicting classifications of pathogenicity Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
RS778307537 Health Risk Conflicting classifications of pathogenicity Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
RS781268909 Health Risk Conflicting classifications of pathogenicity Perry syndrome, Neuronopathy, distal hereditary motor
RS886039228 Health Risk Conflicting classifications of pathogenicity Perry syndrome, Amyotrophic lateral sclerosis type 1, Perry syndrome
RS886043620 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS886056328 Health Risk Conflicting classifications of pathogenicity Perry syndrome, Neuronopathy, distal hereditary motor
RS886056332 Health Risk Conflicting classifications of pathogenicity Perry syndrome, Neuronopathy, distal hereditary motor
RS886056333 Health Risk Conflicting classifications of pathogenicity Neuronopathy, distal hereditary motor, type 7B
RS969899022 Health Risk Conflicting classifications of pathogenicity Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
RS1328116832 Health Risk Likely pathogenic Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis
RS1558948987 Health Risk Likely pathogenic Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
RS766653950 Health Risk Likely pathogenic Amyotrophic lateral sclerosis type 1, Neuronopathy, distal hereditary motor
RS886039227 Health Risk Likely pathogenic Perry syndrome, Perry syndrome
RS121909342 Health Risk Pathogenic Neuronopathy, distal hereditary motor, type 7B
RS1553466434 Health Risk Pathogenic Neuronopathy, distal hereditary motor, type 7B
RS2529170080 Health Risk Pathogenic Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
RS67586389 Health Risk Pathogenic Perry syndrome, Neuronopathy, distal hereditary motor
RS72466487 Health Risk Pathogenic Perry syndrome, Perry syndrome
RS1675325580 Health Risk Pathogenic/Likely pathogenic Amyotrophic lateral sclerosis type 1, Perry syndrome, Neuronopathy
RS121909343 Health Risk Uncertain significance; risk factor Amyotrophic lateral sclerosis, susceptibility to, Perry syndrome
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