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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Smarcad1 and Sclerotylosis 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 SMARCAD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 8 papers in RGD have been used to annotate Smarcad1


    • An association has been curated linking Smarcad1 and Sclerotylosis 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 SMARCAD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 8 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:25741868 PMID:29409814 PMID:4298032 PMID:8731679


    • An association has been curated linking Smarcad1 and Sclerotylosis 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 SMARCAD1 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Sclerotylosis  (DOID:9001225)
  • 8 papers in RGD have been used to annotate Smarcad1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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