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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking GTF2IRD2B 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:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens) & RGD:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens) & RGD:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens) & RGD:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens) & RGD:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens) & RGD:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens) & RGD:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens) & RGD:155922091|RGD:156041583|RGD:156238361|RGD:156261572|RGD:156283481|RGD:329353391|RGD:401862140|RGD:401893870 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate GTF2IRD2B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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