Send us a Message



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

GENE - TERM ANNOTATION REPORT

92 Annotations Found.

An association has been curated linking USH1G and Usher syndrome type 1G 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:28902897 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8610989 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:16283141 PMID:20142502 PMID:24033266 PMID:25741868 PMID:28492532 PMID:28944237


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11625522 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:13540482 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8610993 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:17896313 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:9690094 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:22135276 PMID:24033266 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8610992 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:17896313 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8557092 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:12588794


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8557091 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:12588794


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8568913 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:21044053


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8595961 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:12588794


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8595962 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:11941484 PMID:12588794 PMID:25741868


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:9689713 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:26886449 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:14689878 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:14693136 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28906272 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28897450 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11622379 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11632171 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28906845 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28900304 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28900315 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11618954 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28900303 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28900312 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28907085 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11628475 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28907082 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28897447 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28907080 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11644866 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11626339 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11630530 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11623009 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28907307 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28897711 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11660985 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28900310 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8610996 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8611001 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:17896313 PMID:22135276 PMID:24033266 PMID:25741868 PMID:28224992 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28907079 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11613294 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28900534 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28900307 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28897443 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11658473 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11625564 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11621094 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11651067 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11657015 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28897708 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11631786 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8610994 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11618464 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28906274 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11658288 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11656574 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11631355 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11663570 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11630827 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28906277 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11091020 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:17896313 PMID:24033266


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11629258 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11625083 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11627337 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11629491 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28897714 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28906276 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8610988 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:23591405 PMID:24033266 PMID:25741868 PMID:26878454 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11640727 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:13797608 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:25741868 PMID:30303587


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:243056249 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:35802133 PMID:36633841


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:243056251 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:35802133 PMID:36633841


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:150547047 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:152999348 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11628539 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1G
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11090300 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: USH1G-related condition
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:9688264 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: USH1G-Related Disorders
  • Original References(s): PMID:24033266 PMID:25255398 PMID:25741868 PMID:27068579 PMID:27353947 PMID:28492532 PMID:30245029 PMID:30311386 PMID:30828346 PMID:31637240


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:26892330 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:12588794 PMID:22219650 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:26888281 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:150547045 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28907301 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:17896313 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:150507729 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:38476340 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:28907303 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:11633374 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:12588794 PMID:22219650 PMID:28492532 PMID:28944237


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:8595963 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:12588794 PMID:15660226 PMID:22219650 PMID:28492532


  • An association has been curated linking USH1G and Usher syndrome type 1G 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:126772004 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1G
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:33095980 PMID:33946315 PMID:9536098


  • An association has been curated linking USH1G and Usher syndrome type 1G in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking USH1G and Usher syndrome type 1G in Homo sapiens.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Ush1g (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Usher syndrome type 1G  (DOID:0110834)
  • 7 papers in RGD have been used to annotate USH1G
  • Curation Notes: OMIM:606943


  • Go Back to source page   Continue to Ontology report