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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking MIR638 and Charcot-Marie-Tooth disease dominant intermediate B 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:151827506 (Homo sapiens)
  • 94 RGD objects have been annotated to Charcot-Marie-Tooth disease dominant intermediate B  (DOID:0110197)
  • 1 papers in RGD have been used to annotate MIR638
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease dominant intermediate B
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


    • An association has been curated linking MIR638 and Charcot-Marie-Tooth disease dominant intermediate B 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:13610145 (Homo sapiens)
  • 94 RGD objects have been annotated to Charcot-Marie-Tooth disease dominant intermediate B  (DOID:0110197)
  • 1 papers in RGD have been used to annotate MIR638
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease dominant intermediate B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking MIR638 and Charcot-Marie-Tooth disease dominant intermediate B 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:127282496|RGD:14716506|RGD:15117423|RGD:152039093|RGD:156006615 (Homo sapiens) & RGD:127282496|RGD:14716506|RGD:15117423|RGD:152039093|RGD:156006615 (Homo sapiens) & RGD:127282496|RGD:14716506|RGD:15117423|RGD:152039093|RGD:156006615 (Homo sapiens) & RGD:127282496|RGD:14716506|RGD:15117423|RGD:152039093|RGD:156006615 (Homo sapiens) & RGD:127282496|RGD:14716506|RGD:15117423|RGD:152039093|RGD:156006615 (Homo sapiens)
  • 94 RGD objects have been annotated to Charcot-Marie-Tooth disease dominant intermediate B  (DOID:0110197)
  • 1 papers in RGD have been used to annotate MIR638
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease dominant intermediate B
  • Original References(s): PMID:28492532


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