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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Nefl and Charcot-Marie-Tooth disease type 1F in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with NEFL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 64 papers in RGD have been used to annotate Nefl


    • An association has been curated linking Nefl and Charcot-Marie-Tooth disease type 1F 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 NEFL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 64 papers in RGD have been used to annotate Nefl
  • Curation Notes: ClinVar Annotator: match by term: CMT 1F | ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F | ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, demyelinating, type 1f
  • Original References(s): PMID:12477167 PMID:12481988 PMID:12566280 PMID:15111691 PMID:16452125 PMID:16930284 PMID:17052987 PMID:18023247 PMID:19123978 PMID:19158810 PMID:19286384 PMID:20039262 PMID:20301384 PMID:20421365 PMID:21168446 PMID:21493625 PMID:21840889 PMID:2288874 PMID:23230147 PMID:24078732 PMID:25448007 PMID:25552649 PMID:25741868 PMID:25741869 PMID:26467025 PMID:26645395 PMID:27206872 PMID:28492532 PMID:28501821 PMID:31211173 PMID:31574566 PMID:31673878


    • An association has been curated linking Nefl and Charcot-Marie-Tooth disease type 1F 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 NEFL (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 64 papers in RGD have been used to annotate Nefl
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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