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GENE - TERM ANNOTATION REPORT

123 Annotations Found.

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 Ohki K, etal., Int J Oral Maxillofac Surg. 2004 Sep;33(6):584-92.
  • The annotation has been inferred from sequence orthology with PTCH1 (Homo sapiens) [(IEP) inferred from expression pattern]
  • 8 additional annotations were made from Ohki K, etal., Int J Oral Maxillofac Surg. 2004 Sep;33(6):584-92.
  • 10 CRRD objects have been annotated to nevoid basal cell carcinoma syndrome  (DOID:2512)
  • 40 papers in CRRD have been used to annotate Ptch1


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22703879, PMID:28492532


  • 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.
  • 10 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 Rattus norvegicus.        

  • 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:24728327, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:25741868, PMID:28492532


  • 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 Feng W, etal., Genesis. 2013 Oct;51(10):677-89. doi: 10.1002/dvg.22416. Epub 2013 Aug 30.
  • The annotation has been inferred from sequence orthology with Ptch1 (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Feng W, etal., Genesis. 2013 Oct;51(10):677-89. doi: 10.1002/dvg.22416. Epub 2013 Aug 30.
  • 10 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: splice-site mutation :exon


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:26893459, PMID:28492532


  • 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 OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 CRRD objects have been annotated to nevoid basal cell carcinoma syndrome  (DOID:2512)
  • 40 papers in CRRD have been used to annotate Ptch1


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:25637381, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by OMIM:109400
  • Original References(s): PMID:26544948


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by OMIM:109400
  • Original References(s): PMID:25741868


  • 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 Takahashi C, etal., J Hum Genet. 2009 Jul;54(7):403-8. doi: 10.1038/jhg.2009.55. Epub 2009 Jun 26.
  • 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 Takahashi C, etal., J Hum Genet. 2009 Jul;54(7):403-8. doi: 10.1038/jhg.2009.55. Epub 2009 Jun 26.
  • 10 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: nonsense mutation:exon:p.W399* (human)


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by OMIM:109400
  • Original References(s): PMID:8658145


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by OMIM:109400
  • Original References(s): PMID:8681379


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by OMIM:109400


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by OMIM:109400
  • Original References(s): PMID:12900905, PMID:18477452


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:29575684, PMID:8681379


  • 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 Zhang T, etal., Biochem Biophys Res Commun. 2011 Jun 3;409(2):166-70. doi: 10.1016/j.bbrc.2011.04.047. Epub 2011 Apr 13.
  • 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 Zhang T, etal., Biochem Biophys Res Commun. 2011 Jun 3;409(2):166-70. doi: 10.1016/j.bbrc.2011.04.047. Epub 2011 Apr 13.
  • 10 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:missense mutation:exon:p.E237EK (897G>A) (human)


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Basal cell nevus syndrome
  • Original References(s): PMID:23313819, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:9341860


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Fifth Phacomatosis
  • Original References(s): PMID:28492532, PMID:30311386


  • 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 RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PTCH1 (Homo sapiens) [(EXP) inferred from experiment]
  • 10 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: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:16405370, PMID:16936257, PMID:18539553, PMID:19287498, PMID:25559776, PMID:25876211


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Basal cell nevus syndrome
  • Original References(s): PMID:18502968, PMID:23313819, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16419085, PMID:17021131, PMID:28492532, PMID:8658145, PMID:8981943


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:17021131, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:18502968, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16301862, PMID:16419085, PMID:24814739, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:25567908, PMID:26802149, PMID:26893459, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:12925203, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11941477, PMID:22313357, PMID:22703879, PMID:22995991, PMID:24204797, PMID:24728327, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16508594, PMID:18510667, PMID:25637381, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:15459969, PMID:15712338, PMID:27561271, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:15712338, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:28733979


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:25741868, PMID:28492532, PMID:31837199


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:12192414, PMID:12655573, PMID:15042702, PMID:15712338, PMID:16088933, PMID:16203740, PMID:16301862, PMID:19557015, PMID:24204797, PMID:28492532, PMID:8840969


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11941477, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:29212164, PMID:29654263


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22703879, PMID:23061468, PMID:26893459, PMID:27028851, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:21520333, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:30411536


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:18830227, PMID:21567912, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22703879, PMID:24728327, PMID:25260786, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:20485063, PMID:22703879, PMID:24728327, PMID:28492532, PMID:29575684


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:28596197


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22572734, PMID:24204797, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:24728327, PMID:26893459, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:1347096, PMID:26893459, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22703879, PMID:24728327, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:8658145


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:23951062, PMID:24728327, PMID:26544948, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22703879, PMID:24942795, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:12204003, PMID:22703879, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:29575684, PMID:30166346


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:15712338, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16931872, PMID:24204797, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:20068110, PMID:24668667, PMID:24728327, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16909134, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:12204003, PMID:24728327, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:12925203, PMID:28492532, PMID:29575684


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:24668667, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16301862, PMID:16419085, PMID:27561271, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11231326, PMID:23951062, PMID:28492532, PMID:8840969


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16301862, PMID:16419085, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:27535533, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28342698, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11941477, PMID:12879481, PMID:15545745, PMID:17001668, PMID:24204797, PMID:24529220, PMID:25403219, PMID:26356331, PMID:26604511, PMID:8840969, PMID:8981943, PMID:9096761, PMID:9231911


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:25326635, PMID:25741868


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:8981943


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:9415689


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16301862, PMID:28492532, PMID:8981943


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11941477, PMID:12879481, PMID:15545745, PMID:17001668, PMID:22703879, PMID:24204797, PMID:24529220, PMID:25403219, PMID:26356331, PMID:26604511, PMID:28492532, PMID:8840969, PMID:8981943, PMID:9096761, PMID:9231911


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:8681379


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:29212164


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:26544948, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:19002359, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11457640, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22952776, PMID:28492532, PMID:8981943


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16301862, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:24204797, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:25637381, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22382802, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16508594, PMID:18502968, PMID:28492532, PMID:8981943, PMID:9415689


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:18302678, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11231326, PMID:23951062, PMID:26544948, PMID:28492532, PMID:8840969


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11941477, PMID:17096318, PMID:22703879, PMID:24728327, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:21520333, PMID:22675565, PMID:24368541, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:24335643, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:12925203, PMID:15712338, PMID:24728327, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:29575684, PMID:8981943


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22703879, PMID:24033266, PMID:24728327, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:15565302, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:20301330, PMID:25131638, PMID:25741868


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:24728327, PMID:25741868, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:24814739, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22829011, PMID:25117323, PMID:28492532, PMID:8981943


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:26997948, PMID:27561271, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:10200051, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:17001668, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:29983323


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16088933, PMID:16301862, PMID:16419085, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:17703323, PMID:22382802, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:29575684


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:9620294


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:21188540, PMID:22703879, PMID:24728327, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11941477, PMID:19346217, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:11941477, PMID:17001668, PMID:21188540, PMID:22703879, PMID:22820256, PMID:24055113, PMID:24728327, PMID:25637381, PMID:26489027, PMID:26893459, PMID:27153395, PMID:28492532, PMID:8302318


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:27793025, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:10048928, PMID:15459969, PMID:16929110, PMID:18373848, PMID:21520333, PMID:28492532, PMID:29575684


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16508594, PMID:25525159, PMID:25637381, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:27930734, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16088933, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:27561271, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:28873162


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:10564585, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:23951062, PMID:26544948, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:22703879, PMID:24728327, PMID:28492532, PMID:9463336


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:25741868, PMID:28492532, PMID:28873162


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16301862, PMID:16419085, PMID:28492532, PMID:29575684


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:28492532, PMID:28690523


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:23761049, PMID:28492532


  • 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 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 PTCH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 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: ClinVar Annotator: match by term: Gorlin syndrome
  • Original References(s): PMID:16231297, PMID:23334667, PMID:24728327, PMID:26893459, PMID:28492532


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