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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FGFR1 and Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with FGFR1 (Homo sapiens)
  • 1 RGD objects have been annotated to Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant  (DOID:9001871)
  • 0 papers in RGD have been used to annotate FGFR1
  • Curation Notes: DNA:missense mutations, nonsense mutations:exon:multiple
  • Original References(s): PMID:16764984 REF_RGD_ID:11567241


  • An association has been curated linking FGFR1 and Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with FGFR1 (Homo sapiens)
  • 1 RGD objects have been annotated to Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant  (DOID:9001871)
  • 0 papers in RGD have been used to annotate FGFR1
  • Curation Notes: DNA:frameshift mutation, missense mutations: :multiple
  • Original References(s): PMID:16882753 REF_RGD_ID:11567239


  • An association has been curated linking FGFR1 and Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with FGFR1 (Homo sapiens)
  • 1 RGD objects have been annotated to Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant  (DOID:9001871)
  • 0 papers in RGD have been used to annotate FGFR1
  • Curation Notes: DNA:missense mutation, nonsense mutation:exon:p.S107X (320C>A), p.G687R (2059G>A) (human)
  • Original References(s): PMID:15845591 REF_RGD_ID:11567240


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