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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking IRF8 and genetic disease 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:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens) & RGD:155922500|RGD:155932541|RGD:155991148|RGD:156257522|RGD:401725457|RGD:401773109|RGD:405801055|RGD:407458236|RGD:407458238 (Homo sapiens)
  • 27296 RGD objects have been annotated to genetic disease  (DOID:630)
  • 16 papers in RGD have been used to annotate IRF8
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking IRF8 and genetic disease 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:151849214|RGD:155944110|RGD:26885252|RGD:38489260|RGD:38498893|RGD:401721302 (Homo sapiens) & RGD:151849214|RGD:155944110|RGD:26885252|RGD:38489260|RGD:38498893|RGD:401721302 (Homo sapiens) & RGD:151849214|RGD:155944110|RGD:26885252|RGD:38489260|RGD:38498893|RGD:401721302 (Homo sapiens) & RGD:151849214|RGD:155944110|RGD:26885252|RGD:38489260|RGD:38498893|RGD:401721302 (Homo sapiens) & RGD:151849214|RGD:155944110|RGD:26885252|RGD:38489260|RGD:38498893|RGD:401721302 (Homo sapiens) & RGD:151849214|RGD:155944110|RGD:26885252|RGD:38489260|RGD:38498893|RGD:401721302 (Homo sapiens)
  • 27296 RGD objects have been annotated to genetic disease  (DOID:630)
  • 16 papers in RGD have been used to annotate IRF8
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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