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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking ACTG2 and genetic disease 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:10401603 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 6 papers in RGD have been used to annotate ACTG2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24337657 PMID:24676022 PMID:25741868 PMID:25998219 PMID:26072522 PMID:26813947 PMID:27481187 PMID:31769566


    • An association has been curated linking ACTG2 and genetic disease 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:8688830 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 6 papers in RGD have been used to annotate ACTG2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11474115 PMID:24337657 PMID:24676022 PMID:25998219 PMID:26072522 PMID:26647307 PMID:26813947 PMID:27481187 PMID:31769566


    • An association has been curated linking ACTG2 and genetic disease 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:8688833 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 6 papers in RGD have been used to annotate ACTG2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:23806086 PMID:24088041 PMID:24337657 PMID:24676022 PMID:25741868 PMID:25998219 PMID:26072522 PMID:26813947 PMID:31769566


    • An association has been curated linking ACTG2 and genetic disease 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:155987582|RGD:156295275|RGD:405720996 (Homo sapiens) & RGD:155987582|RGD:156295275|RGD:405720996 (Homo sapiens) & RGD:155987582|RGD:156295275|RGD:405720996 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 6 papers in RGD have been used to annotate ACTG2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking ACTG2 and genetic disease 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:8688835 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 6 papers in RGD have been used to annotate ACTG2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:23806086 PMID:24088041 PMID:24337657 PMID:24676022 PMID:25741868 PMID:25998219 PMID:26072522 PMID:26647307 PMID:26813947 PMID:28422808 PMID:29781137 PMID:31769566 PMID:32814715 PMID:33294969


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