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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking F2 and sensorineural hearing loss in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • The annotation has been inferred from sequence orthology with F2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 606 RGD objects have been annotated to sensorineural hearing loss  (DOID:10003)
  • 152 papers in RGD have been used to annotate F2
  • Qualifier: no_association
  • Curation Notes: DNA:transition: :20210G>A(human)


  • An association has been curated linking F2 and sensorineural hearing loss in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 8 additional annotations were made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 606 RGD objects have been annotated to sensorineural hearing loss  (DOID:10003)
  • 141 papers in RGD have been used to annotate F2
  • Qualifier: no_association
  • Curation Notes: DNA:transition: :20210G>A(human)


  • An association has been curated linking F2 and sensorineural hearing loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • The annotation has been inferred from sequence orthology with F2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 606 RGD objects have been annotated to sensorineural hearing loss  (DOID:10003)
  • 145 papers in RGD have been used to annotate F2
  • Qualifier: no_association
  • Curation Notes: DNA:transition: :20210G>A(human)


  • An association has been curated linking F5 and sensorineural hearing loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • The annotation has been inferred from sequence orthology with F5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 606 RGD objects have been annotated to sensorineural hearing loss  (DOID:10003)
  • 71 papers in RGD have been used to annotate F5
  • Qualifier: no_association
  • Curation Notes: DNA:SNP: :1691G>A (human)


  • An association has been curated linking F5 and sensorineural hearing loss in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 8 additional annotations were made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 606 RGD objects have been annotated to sensorineural hearing loss  (DOID:10003)
  • 67 papers in RGD have been used to annotate F5
  • Qualifier: no_association
  • Curation Notes: DNA:SNP: :1691G>A (human)


  • An association has been curated linking F5 and sensorineural hearing loss in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • The annotation has been inferred from sequence orthology with F5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Cadoni G, etal., Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.
  • 606 RGD objects have been annotated to sensorineural hearing loss  (DOID:10003)
  • 71 papers in RGD have been used to annotate F5
  • Qualifier: no_association
  • Curation Notes: DNA:SNP: :1691G>A (human)


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