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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

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

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Soltanpour MS, etal., J Res Med Sci. 2013 Jun;18(6):487-91.
  • 4 additional annotations were made from Soltanpour MS, etal., J Res Med Sci. 2013 Jun;18(6):487-91.
  • 19 RGD objects have been annotated to retinal vein occlusion  (DOID:1727)
  • 164 papers in RGD have been used to annotate MTHFR
  • Qualifier: no_association
  • Curation Notes: DNA:missense mutation:cds:677C>T (human)


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

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Soltanpour MS, etal., J Res Med Sci. 2013 Jun;18(6):487-91.
  • The annotation has been inferred from sequence orthology with MTHFR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Soltanpour MS, etal., J Res Med Sci. 2013 Jun;18(6):487-91.
  • 19 RGD objects have been annotated to retinal vein occlusion  (DOID:1727)
  • 171 papers in RGD have been used to annotate Mthfr
  • Qualifier: no_association
  • Curation Notes: DNA:missense mutation:cds:677C>T (human)


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

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Soltanpour MS, etal., J Res Med Sci. 2013 Jun;18(6):487-91.
  • The annotation has been inferred from sequence orthology with MTHFR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Soltanpour MS, etal., J Res Med Sci. 2013 Jun;18(6):487-91.
  • 19 RGD objects have been annotated to retinal vein occlusion  (DOID:1727)
  • 158 papers in RGD have been used to annotate Mthfr
  • Qualifier: no_association
  • Curation Notes: DNA:missense mutation:cds:677C>T (human)


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