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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking USH2A-AS1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:21738395 PMID:24033266 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A-AS1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A-AS1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13435444 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A-AS1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126923385 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25425308 PMID:25741868 PMID:28492532 PMID:29940899 PMID:31054281 PMID:32188678 PMID:34781295


  • An association has been curated linking USH2A-AS1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611357 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28041643


  • An association has been curated linking USH2A-AS1 and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 0 papers in RGD have been used to annotate USH2A-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • 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


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