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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking HSPA2-AS1 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:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens) & RGD:155966366|RGD:156056161|RGD:156059217|RGD:156082281|RGD:156132095|RGD:156164567|RGD:156183776|RGD:156244964|RGD:156250178|RGD:156295529|RGD:156342177|RGD:329397364|RGD:401725687|RGD:401759713 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate HSPA2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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