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GENE - TERM ANNOTATION REPORT

161 Annotations Found.

An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26910030 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:22135276 PMID:24944099 PMID:25741868 PMID:26927203 PMID:28492532 PMID:28981474 PMID:36011334


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:40906307 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13786533 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:22004887 PMID:24160897 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13783504 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11578745 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:151717564 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13782798 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8568541 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:22009552


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11580289 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13788828 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13783976 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:19737284


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11581115 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13782756 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:27460420


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13788900 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13216720 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13792219 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9480365 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9480366 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611369 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:20301442 PMID:21569298 PMID:24033266 PMID:25741868 PMID:26927203 PMID:28041643 PMID:28492532 PMID:30245029


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13804587 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13791684 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16963483 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:28887631 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9688280 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13435429 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611362 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611355 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:21147909 PMID:24033266 PMID:25468891 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11351249 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9690242 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26927203 PMID:27208204 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38465761 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:12895566 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611368 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:10050469 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9692607 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:150338828 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9692609 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:15325563 PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26902570 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9688278 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9688279 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:21738395 PMID:24033266 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:150338827 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:28887928 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611370 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:10729113 PMID:11311042 PMID:15241801 PMID:22004887 PMID:22135276 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:150338826 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611365 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11578239 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26897928 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:15179156 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38462469 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:40906308 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:15124734 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11656209 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:15162629 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:15189074 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11645357 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13791706 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24265693 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13435091 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15325563 PMID:20507924 PMID:25649381 PMID:25741868 PMID:26856745 PMID:27460420 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11579221 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:152078461 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611371 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:16963483 PMID:20591486 PMID:24033266 PMID:24154662 PMID:25097241 PMID:25472526 PMID:25741868 PMID:25804404 PMID:26075083 PMID:26927203 PMID:27957503 PMID:28492532 PMID:28981474 PMID:30245029 PMID:31047384 PMID:31429209 PMID:34906470


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:150454035 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:15191188 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611359 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:24033266 PMID:25472526 PMID:25649381 PMID:25741868 PMID:27460420 PMID:27957503 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126731991 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:127276369 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126735469 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26900568 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:127253093 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38489334 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126771058 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:15119613 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126745933 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126748200 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126733089 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:15139221 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38482959 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126737547 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:21070568 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2A
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:156385740 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155643351 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155723832 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155723230 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155735603 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155729088 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155735747 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155737043 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155724632 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13837558 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:28492532 PMID:35076463


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155736440 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155722510 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155723723 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155682595 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611360 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26899662 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25558175 PMID:25649381 PMID:25741868 PMID:28492532 PMID:30073356


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155735266 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11580024 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9691057 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26927203 PMID:28224992 PMID:28492532 PMID:30902645 PMID:31877679 PMID:32176120 PMID:34148116


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38470499 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25366773 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8689249 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:22135276 PMID:25741868 PMID:25991456 PMID:27208204 PMID:27460420 PMID:27957503 PMID:28492532 PMID:28512305 PMID:30718709


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13782968 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15823922 PMID:20507924 PMID:21569298 PMID:24944099 PMID:25525159 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38463679 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:21151602 PMID:25741868 PMID:28492532 PMID:28894305


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126915624 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:16963483 PMID:17576681 PMID:25741868 PMID:28492532 PMID:32037395 PMID:9536098


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13435005 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:23591405 PMID:25741868 PMID:28041643 PMID:28492532 PMID:33926394


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26910679 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:17405132 PMID:20507924 PMID:23591405 PMID:25649381 PMID:25741868 PMID:27460420 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611366 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13790660 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16963483 PMID:20507924 PMID:25525159 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611364 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:20613545 PMID:24033266 PMID:25649381 PMID:25741868 PMID:27318125 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13787963 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:23967202 PMID:25078356 PMID:25741868 PMID:28492532 PMID:33946315


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11639727 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:14703962 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13787794 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24944099 PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:12838762 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:156179034 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13791785 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:127266624 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:151779421 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532 PMID:30826590 PMID:31144483 PMID:32093671 PMID:32675063 PMID:33124170 PMID:33781268


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:12906022 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:156213206 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126768412 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13522191 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:150330479 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:28877722 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20301515 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8696094 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38491819 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26900626 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:151837162 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26910982 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26909282 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13445766 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:151828201 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13791533 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:15325563 PMID:20507924 PMID:22952768 PMID:25741868 PMID:28492532 PMID:31456290


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:21067039 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:16963483 PMID:21738395 PMID:24367894 PMID:25741868 PMID:25999674 PMID:26927203 PMID:28492532 PMID:28559085 PMID:32098976 PMID:33111345 PMID:33576794


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:151233653 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:30543658 PMID:9536098


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:150453293 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9692608 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:152041757 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:12895147 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:26969326


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:156310332 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13535280 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611361 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611352 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13783374 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:24033266 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126920602 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26909325 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:38463190 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:9692606 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11093334 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13537388 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26900350 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25366773 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:156062173 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:14396699 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26899398 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8556755 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15325563 PMID:19683999 PMID:20507924 PMID:24033266 PMID:25649381 PMID:25741868 PMID:28492532 PMID:9624053


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:155936630 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:126914811 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28559085


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:26901335 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:151881949 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:8611358 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:28897121 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:151802727 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:12845382 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:11559761 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15325563 PMID:18641288 PMID:19881469 PMID:20507924 PMID:22135276 PMID:23924366 PMID:24033266 PMID:25472526 PMID:25649381 PMID:25741868 PMID:27624628 PMID:28492532 PMID:32037395 PMID:34203967


  • An association has been curated linking USH2A-AS1 and Usher syndrome type 2A 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:13787584 (Homo sapiens)
  • 12 RGD objects have been annotated to Usher syndrome type 2A  (DOID:0110838)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
  • Original References(s): PMID:25078356 PMID:25741868 PMID:28492532 PMID:31213501 PMID:33105608 PMID:33629268


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