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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking ARRB2 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:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens) & RGD:156053695|RGD:156072034|RGD:156189811|RGD:156220369|RGD:156254388|RGD:156295613|RGD:329401655|RGD:401733417|RGD:401737393|RGD:401757624|RGD:401771113|RGD:401778061|RGD:401781942|RGD:401883897 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 38 papers in RGD have been used to annotate ARRB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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