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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking SMARCAD1 and Sclerotylosis in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 6 papers in RGD have been used to annotate SMARCAD1


    • An association has been curated linking SMARCAD1 and Sclerotylosis 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:14396286 (Homo sapiens)
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 6 papers in RGD have been used to annotate SMARCAD1
  • Curation Notes: ClinVar Annotator: match by term: Keratoderma with scleroatrophy of the extremities
  • Original References(s): PMID:29409814 PMID:8731679


    • An association has been curated linking SMARCAD1 and Sclerotylosis 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:14396287 (Homo sapiens)
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 6 papers in RGD have been used to annotate SMARCAD1
  • Curation Notes: ClinVar Annotator: match by term: Keratoderma with scleroatrophy of the extremities
  • Original References(s): PMID:29409814 PMID:4298032


    • An association has been curated linking SMARCAD1 and Sclerotylosis 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:9854612 (Homo sapiens)
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 6 papers in RGD have been used to annotate SMARCAD1
  • Curation Notes: ClinVar Annotator: match by term: Keratoderma with scleroatrophy of the extremities
  • Original References(s): PMID:10631162 PMID:24909267 PMID:29409814


    • An association has been curated linking SMARCAD1 and Sclerotylosis in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 6 papers in RGD have been used to annotate SMARCAD1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking SMARCAD1 and Sclerotylosis 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:150442739|RGD:150452883|RGD:150495623|RGD:150504122 (Homo sapiens) & RGD:150442739|RGD:150452883|RGD:150495623|RGD:150504122 (Homo sapiens) & RGD:150442739|RGD:150452883|RGD:150495623|RGD:150504122 (Homo sapiens) & RGD:150442739|RGD:150452883|RGD:150495623|RGD:150504122 (Homo sapiens)
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 6 papers in RGD have been used to annotate SMARCAD1
  • Curation Notes: ClinVar Annotator: match by term: Keratoderma with scleroatrophy of the extremities
  • Original References(s): PMID:25741868


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