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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:8609314 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:150338769 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:25741868


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:12740259 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:13791916 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:13485414 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33111345


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:28909520 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:28492532


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:13782912 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:28492532


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:38465757 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:25741868


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:11095903 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking AL353784.1 and Usher syndrome type 1F 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:13784226 (Homo sapiens)
  • 4 RGD objects have been annotated to Usher syndrome type 1F  (DOID:0110832)
  • 0 papers in RGD have been used to annotate AL353784.1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1F
  • Original References(s): PMID:25741868 PMID:26166082


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