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GENE - TERM ANNOTATION REPORT

101 Annotations Found.

An association has been curated linking CLRN1 and Usher syndrome type 3 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:13784706 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:30311386


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11093085 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:20717163 PMID:24033266 PMID:25741868 PMID:27460420 PMID:30311386


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13782552 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13784266 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8558072 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:12080385 PMID:12145752 PMID:14569126 PMID:16028794 PMID:18281613 PMID:19423712 PMID:19753315 PMID:22787034 PMID:24033266 PMID:25741868 PMID:26180195 PMID:28041643 PMID:28492532 PMID:34906470


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13785458 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8558074 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:11524702 PMID:12080385 PMID:15521980 PMID:23304067 PMID:24033266 PMID:24498627 PMID:24596593 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8611010 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:22135276 PMID:24033266 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8611009 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:12080385 PMID:12145752 PMID:15521980 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13838558 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8558071 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:11524702 PMID:12145752


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:21404306 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:25741868


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13788852 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875129 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11585114 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:25741868


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13786715 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875123 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875125 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:21404928 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13791982 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8558075 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:12080385


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28873065 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13785988 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13783078 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:15169100 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11588090 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11665918 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11584792 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13784737 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11644583 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875128 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13792304 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:14695560 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:25741868


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28905082 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28873344 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11589045 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875133 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28873060 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11594728 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11591732 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11584364 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13792069 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13785252 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28885414 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13785009 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:9693537 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11589725 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875335 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875331 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28905079 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11584005 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13785111 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28905076 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11666407 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11665861 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11589837 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:21404927 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28873336 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11665445 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13786765 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13791696 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28873058 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875339 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11588517 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11592864 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28875334 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11585638 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:38465753 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28873063 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:12740574 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13789391 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11582505 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11583064 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:26919363 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13519694 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:11093911 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:12739149 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:22952768 PMID:23304067 PMID:25741868 PMID:26338283 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8558069 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:11524702 PMID:12145752 PMID:19753315 PMID:22681893 PMID:24033266 PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28873339 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • 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 type 3 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:11586512 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13785386 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:25268133 PMID:27610647 PMID:28471114 PMID:28492532 PMID:31213501 PMID:31960602


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:38484309 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:15111292 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:38481065 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:126753920 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:126758987 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:14394085 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:26885993 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:21067086 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • 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 type 3 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:13540413 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:22952768 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:14746576 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:17576681 PMID:22952768 PMID:23304067 PMID:25741868 PMID:26338283 PMID:28492532 PMID:9536098


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • 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 type 3 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)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:11524702 PMID:21675857 PMID:24033266 PMID:24498627 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8611005 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:12080385 PMID:12145752 PMID:14569126 PMID:18281613 PMID:19423712 PMID:19753315 PMID:22787034 PMID:24033266 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8558070 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:11524702 PMID:12145752 PMID:19753315 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:13791368 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:8558073 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:12145752 PMID:25741868


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:12740507 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:11524702 PMID:24498627 PMID:25741868 PMID:28492532


  • An association has been curated linking CLRN1 and Usher syndrome type 3 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:28905085 (Homo sapiens)
  • 7 RGD objects have been annotated to Usher syndrome type 3  (DOID:0110828)
  • 7 papers in RGD have been used to annotate CLRN1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:23304067 PMID:28492532


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