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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking IFIT3 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:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens) & RGD:155910850|RGD:155959776|RGD:156039606|RGD:156046673|RGD:156069960|RGD:156098612|RGD:156100966|RGD:156154082|RGD:156154696|RGD:156159716|RGD:156249080|RGD:156334837|RGD:156397396|RGD:329378832|RGD:401756095|RGD:401856099|RGD:401882614|RGD:401882917|RGD:401898693 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 3 papers in RGD have been used to annotate IFIT3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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