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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Nog and multiple synostoses syndrome 1 in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with NOG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to multiple synostoses syndrome 1  (DOID:0081317)
  • 33 papers in RGD have been used to annotate Nog


    • An association has been curated linking Nog and multiple synostoses syndrome 1 in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Declau F, etal., Otol Neurotol. 2005 Sep;26(5):934-40.
  • The annotation has been inferred from sequence orthology with NOG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 additional annotations were made from Declau F, etal., Otol Neurotol. 2005 Sep;26(5):934-40.
  • 3 RGD objects have been annotated to multiple synostoses syndrome 1  (DOID:0081317)
  • 33 papers in RGD have been used to annotate Nog
  • Curation Notes: DNA:mutation:cds:1426G>C (P.W205C)(Human)


    • An association has been curated linking Nog and multiple synostoses syndrome 1 in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Gong Y, etal., Nat Genet. 1999 Mar;21(3):302-4.
  • The annotation has been inferred from sequence orthology with NOG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Gong Y, etal., Nat Genet. 1999 Mar;21(3):302-4.
  • 3 RGD objects have been annotated to multiple synostoses syndrome 1  (DOID:0081317)
  • 33 papers in RGD have been used to annotate Nog


    • An association has been curated linking Nog and multiple synostoses syndrome 1 in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to multiple synostoses syndrome 1  (DOID:0081317)
  • 33 papers in RGD have been used to annotate Nog
  • Curation Notes: ClinVar Annotator: match by term: Symphalangism-brachydactyly syndrome
  • Original References(s): PMID:10080184 PMID:11846737 PMID:15770128 PMID:16532400 PMID:17609215 PMID:20503332 PMID:25741868 PMID:30311386 PMID:3667255 PMID:6638061


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