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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking BSND and Bartter disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Birkenhager R, etal., Nat Genet. 2001 Nov;29(3):310-4.
  • 5 additional annotations were made from Birkenhager R, etal., Nat Genet. 2001 Nov;29(3):310-4.
  • 10 RGD objects have been annotated to Bartter disease  (DOID:445)
  • 6 papers in RGD have been used to annotate BSND
  • Curation Notes: Bartter syndrome with sensorineural deafness, OMIM:602522, DNA:point mutation:A1T, R8W, DNA:deletion:exon


  • An association has been curated linking Bsnd and Bartter disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Birkenhager R, etal., Nat Genet. 2001 Nov;29(3):310-4.
  • The annotation has been inferred from sequence orthology with BSND (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Birkenhager R, etal., Nat Genet. 2001 Nov;29(3):310-4.
  • 10 RGD objects have been annotated to Bartter disease  (DOID:445)
  • 11 papers in RGD have been used to annotate Bsnd
  • Curation Notes: Bartter syndrome with sensorineural deafness, OMIM:602522, DNA:point mutation:A1T, R8W, DNA:deletion:exon


  • An association has been curated linking Bsnd and Bartter disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Birkenhager R, etal., Nat Genet. 2001 Nov;29(3):310-4.
  • The annotation has been inferred from sequence orthology with BSND (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Birkenhager R, etal., Nat Genet. 2001 Nov;29(3):310-4.
  • 10 RGD objects have been annotated to Bartter disease  (DOID:445)
  • 6 papers in RGD have been used to annotate Bsnd
  • Curation Notes: Bartter syndrome with sensorineural deafness, OMIM:602522, DNA:point mutation:A1T, R8W, DNA:deletion:exon


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