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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking VAPA 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:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens) & RGD:156084032|RGD:156088562|RGD:156138262|RGD:156151411|RGD:156241239|RGD:156282809|RGD:156367094|RGD:329360608|RGD:401720616|RGD:401752405|RGD:401756528|RGD:401776764|RGD:401777531|RGD:401778760 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 3 papers in RGD have been used to annotate VAPA
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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