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GENE - TERM ANNOTATION REPORT

28 Annotations Found.

An association has been curated linking ADGRV1 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:13435433 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


    • An association has been curated linking ADGRV1 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:151743781 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ADGRV1 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:151769118 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:25741868 PMID:26667666 PMID:28492532 PMID:30029497 PMID:36555390


    • An association has been curated linking ADGRV1 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:150534999 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:26338283 PMID:28492532 PMID:33089500


    • An association has been curated linking ADGRV1 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:155266277 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22147658 PMID:25404053 PMID:30459346


    • An association has been curated linking ADGRV1 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:126910741 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30311386


    • An association has been curated linking ADGRV1 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:26909709 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32037395 PMID:32467589


    • An association has been curated linking ADGRV1 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:13435443 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:26467025 PMID:28041643 PMID:28492532 PMID:29099798 PMID:30718709 PMID:31047384 PMID:32467589


    • An association has been curated linking ADGRV1 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:8597265 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:14740321 PMID:15671307 PMID:19357117 PMID:22135276 PMID:22147658 PMID:24033266 PMID:25741868 PMID:26164827 PMID:26226137 PMID:27575413 PMID:28041643 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32467589


    • An association has been curated linking ADGRV1 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:127231703 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16199547 PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32467589


    • An association has been curated linking ADGRV1 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:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens) & RGD:14695739|RGD:151236279|RGD:151236280|RGD:153305278|RGD:153346076|RGD:155266566|RGD:156055440|RGD:243056650|RGD:243056699|RGD:329847084|RGD:405281369 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


    • An association has been curated linking ADGRV1 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:13795767 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28951997 PMID:30303587


    • An association has been curated linking ADGRV1 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:151887181 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:28492532 PMID:30459346 PMID:30718709 PMID:31047384 PMID:31736247 PMID:32467589


    • An association has been curated linking ADGRV1 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:25318488 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:24498627 PMID:25741868 PMID:26226137 PMID:27068579 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32467589 PMID:36909829


    • An association has been curated linking ADGRV1 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:401927406|RGD:401927430|RGD:401927451|RGD:401927455|RGD:401927466 (Homo sapiens) & RGD:401927406|RGD:401927430|RGD:401927451|RGD:401927455|RGD:401927466 (Homo sapiens) & RGD:401927406|RGD:401927430|RGD:401927451|RGD:401927455|RGD:401927466 (Homo sapiens) & RGD:401927406|RGD:401927430|RGD:401927451|RGD:401927455|RGD:401927466 (Homo sapiens) & RGD:401927406|RGD:401927430|RGD:401927451|RGD:401927455|RGD:401927466 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking ADGRV1 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:13435423 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:28041643 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32467589


    • An association has been curated linking ADGRV1 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:156140053 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:25741868 PMID:26226137 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32467589


    • An association has been curated linking ADGRV1 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:151773748|RGD:155937999 (Homo sapiens) & RGD:151773748|RGD:155937999 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:26667666 PMID:28492532 PMID:30029497 PMID:32467589


    • An association has been curated linking ADGRV1 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:11640720|RGD:13478228 (Homo sapiens) & RGD:11640720|RGD:13478228 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking ADGRV1 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:155796448 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32037395 PMID:32467589 PMID:35813073


    • An association has been curated linking ADGRV1 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:8609146 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16199547 PMID:19357117 PMID:22135276 PMID:22147658 PMID:24033266 PMID:25741868 PMID:26226137 PMID:28492532 PMID:30718709 PMID:31047384 PMID:31456290 PMID:31980526 PMID:32037395 PMID:32467589 PMID:37798099


    • An association has been curated linking ADGRV1 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:151821769|RGD:26910435 (Homo sapiens) & RGD:151821769|RGD:26910435 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:26226137 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32467589


    • An association has been curated linking ADGRV1 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:8609244 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28041643 PMID:28492532 PMID:32420686 PMID:3258136 PMID:33089500


    • An association has been curated linking ADGRV1 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:11638841 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22147658 PMID:25741868 PMID:26969326 PMID:28492532 PMID:30459346 PMID:33297549


    • An association has been curated linking ADGRV1 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:8609186 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:24154662 PMID:25133751 PMID:25404053 PMID:25741868 PMID:26467025 PMID:27068579 PMID:28041643 PMID:28492532 PMID:32037395 PMID:36553628 PMID:37422204


    • An association has been curated linking ADGRV1 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:13478228|RGD:13489026 (Homo sapiens) & RGD:13478228|RGD:13489026 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29266188


    • An association has been curated linking ADGRV1 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:11640720 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking ADGRV1 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:13435424 (Homo sapiens)
  • 220 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate ADGRV1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19357117 PMID:22135276 PMID:22147658 PMID:24033266 PMID:25741868 PMID:26226137 PMID:28041643 PMID:28492532 PMID:30718709 PMID:31047384 PMID:32467589 PMID:32581362


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