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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Dnm2 and congenital structural myopathy in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with DNM2 (Homo sapiens) [(EXP) inferred from experiment]
  • 141 RGD objects have been annotated to congenital structural myopathy  (DOID:422)
  • 53 papers in RGD have been used to annotate Dnm2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:17376685


  • An association has been curated linking Dnm2 and congenital structural myopathy in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with DNM2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 141 RGD objects have been annotated to congenital structural myopathy  (DOID:422)
  • 53 papers in RGD have been used to annotate Dnm2
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant centronuclear myopathy | ClinVar Annotator: match by term: Congenital fiber-type disproportion myopathy | ClinVar Annotator: match by term: Myotubular myopathy
  • Original References(s): PMID:16199547 PMID:16227997 PMID:17008356 PMID:17825552 PMID:17932957 PMID:18414213 PMID:19130742 PMID:19623537 PMID:19932619 PMID:20227276 PMID:20529869 PMID:20700106 PMID:20817456 PMID:20858595 PMID:20927630 PMID:21221624 PMID:21762456 PMID:22096584 PMID:22369075 PMID:22396310 PMID:22613877 PMID:23338057 PMID:23374900 PMID:23394783 PMID:24016602 PMID:24033266 PMID:24088041 PMID:24135484 PMID:24366529 PMID:24465259 PMID:24728327 PMID:25214167 PMID:25262827 PMID:25326635 PMID:25492887 PMID:25501959 PMID:25741868 PMID:25957634 PMID:26199319 PMID:26273216 PMID:26467025 PMID:26503427 PMID:26633545 PMID:26842864 PMID:26908122 PMID:2734399 PMID:27343996 PMID:27572814 PMID:27698851 PMID:27854218 PMID:28492532 PMID:28676641 PMID:30103202 PMID:32860008 PMID:34008892 PMID:34354735 PMID:34837441


  • An association has been curated linking Dnm2 and congenital structural myopathy in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with DNM2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 141 RGD objects have been annotated to congenital structural myopathy  (DOID:422)
  • 53 papers in RGD have been used to annotate Dnm2
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant centronuclear myopathy | ClinVar Annotator: match by term: Congenital fiber-type disproportion myopathy
  • Original References(s): PMID:16227997 PMID:17008356 PMID:17932957 PMID:18414213 PMID:19130742 PMID:20227276 PMID:20529869 PMID:20817456 PMID:20858595 PMID:20927630 PMID:21221624 PMID:21762456 PMID:22096584 PMID:22369075 PMID:22396310 PMID:22613877 PMID:23338057 PMID:23394783 PMID:24016602 PMID:24033266 PMID:24088041 PMID:24465259 PMID:24728327 PMID:25214167 PMID:25262827 PMID:25326635 PMID:25492887 PMID:25501959 PMID:25741868 PMID:25957634 PMID:26199319 PMID:26273216 PMID:26467025 PMID:26633545 PMID:26842864 PMID:26908122 PMID:2734399 PMID:27343996 PMID:27698851 PMID:27854218 PMID:28492532 PMID:28676641 PMID:30103202 PMID:32860008 PMID:34008892


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