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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Tbce and Kenny-Caffey syndrome type 1 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 TBCE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Kenny-Caffey syndrome type 1  (DOID:0080722)
  • 9 papers in RGD have been used to annotate Tbce


    • An association has been curated linking Tbce and Kenny-Caffey syndrome type 1 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 TBCE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Kenny-Caffey syndrome type 1  (DOID:0080722)
  • 9 papers in RGD have been used to annotate Tbce
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive Kenny-Caffey syndrome
  • Original References(s): PMID:12389028 PMID:15645691 PMID:16199547 PMID:2001103 PMID:20152369 PMID:25097779 PMID:25741868 PMID:26231322 PMID:26336027 PMID:27666369 PMID:28492532 PMID:30080992 PMID:30638765 PMID:33652732 PMID:34134906 PMID:34356170 PMID:35432193 PMID:7538982 PMID:9475091


    • An association has been curated linking Tbce and Kenny-Caffey syndrome type 1 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 TBCE (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to Kenny-Caffey syndrome type 1  (DOID:0080722)
  • 9 papers in RGD have been used to annotate Tbce
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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