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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was traceable author statement (TAS)
  •  
  • The annotation was made from Daiger SP, etal., Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19.
  • 152 additional annotations were made from Daiger SP, etal., Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19.
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1


  • An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8611008 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17407589 PMID:19753315 PMID:23304067 PMID:24033266 PMID:25741868 PMID:25743179 PMID:27460420 PMID:28492532 PMID:31097578 PMID:7407589


  • An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:41406227 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8558076 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:15521980 PMID:19753315 PMID:25741868 PMID:28224992 PMID:28492532 PMID:29545425 PMID:31836858 PMID:31963381 PMID:35481838


  • An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:10041454 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17893653 PMID:22952768 PMID:23304067 PMID:25741868 PMID:26338283 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8611007 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:11524702 PMID:21675857 PMID:24033266 PMID:24498627 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:38493742 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:151351972 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25472526 PMID:25741868 PMID:26338283 PMID:28492532


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