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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking FETUB 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:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens) & RGD:155907198|RGD:155926750|RGD:155997539|RGD:156044907|RGD:156052698|RGD:156158815|RGD:329383092|RGD:329394366|RGD:401732139|RGD:401778616|RGD:401781953|RGD:401861756|RGD:401898226|RGD:401898738 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate FETUB
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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