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GENE - TERM ANNOTATION REPORT

110 Annotations Found.

An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151754940 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28899907 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456657 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589161 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25299611 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12833325 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589860 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Genetic motor neuron disease
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28900128 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13821397 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584322 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151846967 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28895526 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156087900 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586763 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11591888 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:19506225 PMID:23143281 PMID:25382069 PMID:26467025 PMID:27132499 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11637740 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14713919 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13616258 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588542 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11592850 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593484 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588508 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585745 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11659411 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586522 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11587898 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28899598 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11590194 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11594624 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13809195 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28886006 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11587663 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585696 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28885998 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654462 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589727 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584408 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15135412 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649711 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649314 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653093 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585487 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586098 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644489 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585654 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651289 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15158867 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11547723 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467958 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:23143281 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15134143 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11547650 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:19506225 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13494115 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13496913 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15194418 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8597915 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:15326253 PMID:18812314 PMID:19506225 PMID:23143281 PMID:25382069 PMID:26467025 PMID:26662454 PMID:27132499 PMID:28430856 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593731 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586530 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28892794 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28885637 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11543496 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551484 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11550764 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:17824900 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580181 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:19506225 PMID:26467025 PMID:28492532 PMID:32028661


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14699631 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: HMN VIIB
  • Original References(s): PMID:25635128 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11587943 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11550584 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589544 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28892219 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28887141 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28887134 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13504286 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:23143281 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8597917 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:15326253 PMID:18812314 PMID:19506225 PMID:23143281 PMID:25025039 PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11640115 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:16199547 PMID:25741868 PMID:28492532 PMID:33369814


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11591909 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:17824900 PMID:19506225 PMID:22777741 PMID:23143281 PMID:25382069 PMID:25741868 PMID:26429889 PMID:26467025 PMID:27132499 PMID:28130640 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551008 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:32402491


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584755 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126740886 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38480514 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126734553 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126739387 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:25741868


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:329355755 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25590979 PMID:25741868


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13483753 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPE VIIB
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583857 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13616248 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28894603 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13491824 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28894298 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8597914 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:12062019 PMID:12627231 PMID:16505168 PMID:18094236 PMID:18364389 PMID:19279216 PMID:23143281 PMID:27573046 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28899593 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13812468 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:23143281 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13804804 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:16199547 PMID:25590979 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11592932 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28166811 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13487242 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28518168 PMID:29525180 PMID:32461654


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650966 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28894609 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584730 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:26742954 PMID:28492532 PMID:28792508 PMID:33973882


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14737652 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401869347 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401856621 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13810203 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28876699 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13616190 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13616194 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585165 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:23143281 PMID:24627108 PMID:25741868 PMID:26392352 PMID:26467025 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401902179 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13616209 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11590347 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11582969 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:28492532


  • An association has been curated linking DCTN1 and autosomal dominant distal hereditary motor neuronopathy 14 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34894200 (Homo sapiens)
  • 11 RGD objects have been annotated to autosomal dominant distal hereditary motor neuronopathy 14  (DOID:0111202)
  • 12 papers in RGD have been used to annotate DCTN1
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type 7B
  • Original References(s): PMID:25741868 PMID:28492532


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