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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking BTK and agammaglobulinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from de Weers M, etal., Hum Mol Genet. 1994 Jan;3(1):161-6.
  • 2 additional annotations were made from de Weers M, etal., Hum Mol Genet. 1994 Jan;3(1):161-6.
  • 102 RGD objects have been annotated to agammaglobulinemia  (DOID:2583)
  • 44 papers in RGD have been used to annotate BTK
  • Qualifier: susceptibility
  • Curation Notes: DNA:insertions, point mutations


    • An association has been curated linking Btk and agammaglobulinemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from de Weers M, etal., Hum Mol Genet. 1994 Jan;3(1):161-6.
  • The annotation has been inferred from sequence orthology with BTK (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from de Weers M, etal., Hum Mol Genet. 1994 Jan;3(1):161-6.
  • 102 RGD objects have been annotated to agammaglobulinemia  (DOID:2583)
  • 49 papers in RGD have been used to annotate Btk
  • Qualifier: susceptibility
  • Curation Notes: DNA:insertions, point mutations


    • An association has been curated linking Btk and agammaglobulinemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from de Weers M, etal., Hum Mol Genet. 1994 Jan;3(1):161-6.
  • The annotation has been inferred from sequence orthology with BTK (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from de Weers M, etal., Hum Mol Genet. 1994 Jan;3(1):161-6.
  • 102 RGD objects have been annotated to agammaglobulinemia  (DOID:2583)
  • 39 papers in RGD have been used to annotate Btk
  • Qualifier: susceptibility
  • Curation Notes: DNA:insertions, point mutations


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