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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking PTCH1 and nevoid basal cell carcinoma syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Boutet N, etal., J Invest Dermatol. 2003 Sep;121(3):478-81.
  • 2 additional annotations were made from Boutet N, etal., J Invest Dermatol. 2003 Sep;121(3):478-81.
  • 12 CRRD objects have been annotated to nevoid basal cell carcinoma syndrome  (DOID:2512)
  • 26 papers in CRRD have been used to annotate PTCH1
  • Curation Notes: DNA:mutations:exon, intron:multiple


  • An association has been curated linking Ptch1 and nevoid basal cell carcinoma syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Boutet N, etal., J Invest Dermatol. 2003 Sep;121(3):478-81.
  • The annotation has been inferred from sequence orthology with PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Boutet N, etal., J Invest Dermatol. 2003 Sep;121(3):478-81.
  • 12 CRRD objects have been annotated to nevoid basal cell carcinoma syndrome  (DOID:2512)
  • 40 papers in CRRD have been used to annotate Ptch1
  • Curation Notes: DNA:mutations:exon, intron:multiple


  • An association has been curated linking Ptch1 and nevoid basal cell carcinoma syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Boutet N, etal., J Invest Dermatol. 2003 Sep;121(3):478-81.
  • The annotation has been inferred from sequence orthology with PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Boutet N, etal., J Invest Dermatol. 2003 Sep;121(3):478-81.
  • 12 CRRD objects have been annotated to nevoid basal cell carcinoma syndrome  (DOID:2512)
  • 27 papers in CRRD have been used to annotate Ptch1
  • Curation Notes: DNA:mutations:exon, intron:multiple


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.