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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking ACP5 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:126914760 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 12 papers in RGD have been used to annotate ACP5
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:27390188 PMID:28492532


    • An association has been curated linking ACP5 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:8555278 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 12 papers in RGD have been used to annotate ACP5
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:13524805 PMID:21217752 PMID:2363422 PMID:25741868 PMID:26951490 PMID:27125509 PMID:28492532


    • An association has been curated linking ACP5 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:13530249 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 12 papers in RGD have been used to annotate ACP5
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:21217752 PMID:21217755 PMID:25741868 PMID:28492532 PMID:28740483


    • An association has been curated linking ACP5 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:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens) & RGD:126912521|RGD:13806545|RGD:14701844|RGD:14735431|RGD:151786868|RGD:151868347|RGD:151880379|RGD:26914068|RGD:26917656|RGD:38457474|RGD:38476483 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 12 papers in RGD have been used to annotate ACP5
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking ACP5 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:155915498|RGD:156275073|RGD:156362245|RGD:401764696 (Homo sapiens) & RGD:155915498|RGD:156275073|RGD:156362245|RGD:401764696 (Homo sapiens) & RGD:155915498|RGD:156275073|RGD:156362245|RGD:401764696 (Homo sapiens) & RGD:155915498|RGD:156275073|RGD:156362245|RGD:401764696 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 12 papers in RGD have been used to annotate ACP5
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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