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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking ERCC8 and Cockayne Syndrome A in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Bertola DR, etal., J Hum Genet. 2006;51(8):701-5. Epub 2006 Jul 25.
  • 2 additional annotations were made from Bertola DR, etal., J Hum Genet. 2006;51(8):701-5. Epub 2006 Jul 25.
  • 3 CRRD objects have been annotated to Cockayne Syndrome A  (DOID:9007866)
  • 11 papers in CRRD have been used to annotate ERCC8
  • Curation Notes: DNA:mutations:multiple (human)


  • An association has been curated linking Ercc8 and Cockayne Syndrome A in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Bertola DR, etal., J Hum Genet. 2006;51(8):701-5. Epub 2006 Jul 25.
  • The annotation has been inferred from sequence orthology with ERCC8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Bertola DR, etal., J Hum Genet. 2006;51(8):701-5. Epub 2006 Jul 25.
  • 3 CRRD objects have been annotated to Cockayne Syndrome A  (DOID:9007866)
  • 15 papers in CRRD have been used to annotate Ercc8
  • Curation Notes: DNA:mutations:multiple (human)


  • An association has been curated linking Ercc8 and Cockayne Syndrome A in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Bertola DR, etal., J Hum Genet. 2006;51(8):701-5. Epub 2006 Jul 25.
  • The annotation has been inferred from sequence orthology with ERCC8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Bertola DR, etal., J Hum Genet. 2006;51(8):701-5. Epub 2006 Jul 25.
  • 3 CRRD objects have been annotated to Cockayne Syndrome A  (DOID:9007866)
  • 16 papers in CRRD have been used to annotate Ercc8
  • Curation Notes: DNA:mutations:multiple (human)


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.