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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Mthfr and Sudden 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 MTHFR (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.
  • 18 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 160 papers in RGD have been used to annotate Mthfr
  • Qualifier: no_association
  • Curation Notes: DNA:SNP:cds:677C>T(human)


    • An association has been curated linking Mthfr and Sudden Hearing Loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Capaccio P, etal., Genet Med. 2005 Mar;7(3):206-8.
  • The annotation has been inferred from sequence orthology with MTHFR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Capaccio P, etal., Genet Med. 2005 Mar;7(3):206-8.
  • 18 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 160 papers in RGD have been used to annotate Mthfr
  • Qualifier: susceptibility
  • Curation Notes: DNA:SNPs:cds:677C>T,1298A>C(human)


    • An association has been curated linking Mthfr and Sudden Hearing Loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Fusconi M, etal., Audiol Neurootol. 2011;16(3):185-90. doi: 10.1159/000319310. Epub 2010 Aug 25.
  • The annotation has been inferred from sequence orthology with MTHFR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Fusconi M, etal., Audiol Neurootol. 2011;16(3):185-90. doi: 10.1159/000319310. Epub 2010 Aug 25.
  • 18 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 160 papers in RGD have been used to annotate Mthfr
  • Curation Notes: DNA:SNP: :677C>T(human)


    • An association has been curated linking Mthfr and Sudden Hearing Loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with MTHFR (Homo sapiens) [(EXP) inferred from experiment]
  • 18 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 160 papers in RGD have been used to annotate Mthfr
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:16275406


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