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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking UGT1A1 and Neonatal Hyperbilirubinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Chang PF, etal., J Pediatr. 2011 Oct;159(4):561-5. doi: 10.1016/j.jpeds.2011.03.042. Epub 2011 May 18.
  • 2 additional annotations were made from Chang PF, etal., J Pediatr. 2011 Oct;159(4):561-5. doi: 10.1016/j.jpeds.2011.03.042. Epub 2011 May 18.
  • 22 RGD objects have been annotated to Neonatal Hyperbilirubinemia  (DOID:9002532)
  • 52 papers in RGD have been used to annotate UGT1A1
  • Qualifier: susceptibility
  • Curation Notes: DNA:polymorphism: :211G>A(human)


    • An association has been curated linking UGT1A1 and Neonatal Hyperbilirubinemia 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
  • 22 RGD objects have been annotated to Neonatal Hyperbilirubinemia  (DOID:9002532)
  • 52 papers in RGD have been used to annotate UGT1A1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:28167773


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