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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking F5 and retinal vein occlusion in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Verity DH, etal., Am J Ophthalmol. 1999 Sep;128(3):352-6.
  • The annotation has been inferred from sequence orthology with F5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Verity DH, etal., Am J Ophthalmol. 1999 Sep;128(3):352-6.
  • 19 RGD objects have been annotated to retinal vein occlusion  (DOID:1727)
  • 71 papers in RGD have been used to annotate F5
  • Curation Notes: associated with Behcet Syndrome;DNA:missense mutation:cds:p.R506Q (human)


  • An association has been curated linking F5 and retinal vein occlusion in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Verity DH, etal., Am J Ophthalmol. 1999 Sep;128(3):352-6.
  • 3 additional annotations were made from Verity DH, etal., Am J Ophthalmol. 1999 Sep;128(3):352-6.
  • 19 RGD objects have been annotated to retinal vein occlusion  (DOID:1727)
  • 67 papers in RGD have been used to annotate F5
  • Curation Notes: associated with Behcet Syndrome;DNA:missense mutation:cds:p.R506Q (human)


  • An association has been curated linking F5 and retinal vein occlusion in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Verity DH, etal., Am J Ophthalmol. 1999 Sep;128(3):352-6.
  • The annotation has been inferred from sequence orthology with F5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Verity DH, etal., Am J Ophthalmol. 1999 Sep;128(3):352-6.
  • 19 RGD objects have been annotated to retinal vein occlusion  (DOID:1727)
  • 71 papers in RGD have been used to annotate F5
  • Curation Notes: associated with Behcet Syndrome;DNA:missense mutation:cds:p.R506Q (human)


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