Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:30311386


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • 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-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • 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-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III
  • Original References(s): PMID:28492532


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher Syndrome, Type III


  • An association has been curated linking CLRN1-AS1 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)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3
  • Original References(s): PMID:11524702 PMID:24498627 PMID:25741868 PMID:28492532


  • Go Back to source page   Continue to Ontology report