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GENE - TERM ANNOTATION REPORT

327 Annotations Found.

An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906938 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906941 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14736542 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Verpy E, etal., Nat Genet. 2000 Sep;26(1):51-5.
  • 4 additional annotations were made from Verpy E, etal., Nat Genet. 2000 Sep;26(1):51-5.
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: DNA:insertion, deletion, repeats:exon, intron:IVS5-2delA, 233-239insC (human)


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905929 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8633965 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093043 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654583 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11550163 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688263 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:22135276 PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11542117 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:27440999


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782790 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24416283 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610844 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791006 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:24498627 PMID:25468891 PMID:25525159 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558494 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:11139240


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8570414 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:16679490 PMID:20142502 PMID:21487335 PMID:21569298 PMID:22135276 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8570415 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:21487335


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8689358 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:21203349 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903602 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558491 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:10973247 PMID:10973248 PMID:11139240 PMID:12107438 PMID:12630964 PMID:12702164 PMID:17407589 PMID:20301442 PMID:21203349 PMID:21569298 PMID:22135276 PMID:24033266 PMID:25741868 PMID:26969326 PMID:28041643 PMID:28492532 PMID:30303587 PMID:30718709


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:12136232


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610880 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608292 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610868 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610871 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787654 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:26445815 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603442 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610890 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13527892 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610843 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787943 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:12136232 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610866 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610841 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610863 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608293 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150330448 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788013 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786667 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784652 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24416283


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783110 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791906 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788986 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783102 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791920 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790009 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787200 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783312 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691063 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787076 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24416283


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690979 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785594 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785515 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785213 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24416283


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792294 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788936 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786600 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786030 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690065 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782569 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790001 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789099 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785958 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791790 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783095 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782417 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786503 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11090354 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788953 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792112 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785432 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610847 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788911 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9692576 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11095496 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783300 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11345566 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:27208204


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784438 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782676 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610883 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786847 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:27460420 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789255 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11091002 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610875 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050084 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:21569298 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785322 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13476258 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715960 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619709 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620255 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14706844 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715956 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715963 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715971 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11604188 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693567 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693565 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13516288 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28909585 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11096372 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150330418 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715944 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905772 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693564 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715953 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782939 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715947 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688552 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150330417 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15126621 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693568 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28906075 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9692578 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15173887 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551170 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15186068 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150330431 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616915 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610877 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:16679490 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28909805 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11549404 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11546566 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14736478 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599268 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617400 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610879 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:11139240 PMID:12702164 PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612934 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610861 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615926 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905773 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616853 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600883 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610873 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551993 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11545197 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610849 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610856 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605727 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616722 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618101 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11545024 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617775 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903438 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620205 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610888 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13540098 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610872 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127282926 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610886 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15146991 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15153635 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15117915 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689785 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28899226 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24618850


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11659887 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905778 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644592 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26917031 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610862 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15130667 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610838 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:24498627 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11091201 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905775 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608294 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906934 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906937 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906943 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26921076 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052795 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906930 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906929 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688551 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610842 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:21203349 PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13516059 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906940 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905923 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606207 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906939 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621330 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906944 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788294 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:22581970 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15115284 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11547571 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11542971 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610839 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151349672 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787002 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906936 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28899233 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38494708 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532 PMID:29625443 PMID:33781268


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150501285 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126766514 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690260 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150459903 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13537242 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126913530 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38470493 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126748296 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15116725 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38490899 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13539865 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26898662 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38471333 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38484908 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126760782 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26919032 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26897161 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15105333 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38471589 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126751270 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126761195 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15142802 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126726667 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126750184 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126923260 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126725128 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126773632 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38466035 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11641008 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126762294 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150333246 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126736243 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26915276 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126733055 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644063 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499636 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126912362 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13519370 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13515237 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38492979 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612544 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610869 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11094707 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784392 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28492532 PMID:32467589


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610864 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13435421 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
  • Original References(s): PMID:28041643 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155797233 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13520115 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:27957503 PMID:28492532 PMID:31858762


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:153345703 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:19297620 PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610857 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:12136232 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29907799 PMID:30096381


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28909803 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558493 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973248 PMID:11139240 PMID:11239869 PMID:11810303 PMID:12630964 PMID:15578223 PMID:15660226 PMID:17174357 PMID:17407589 PMID:18665195 PMID:20095043 PMID:20301442 PMID:20613545 PMID:21436283 PMID:24033266 PMID:25468891 PMID:25741868 PMID:28041643 PMID:28492532 PMID:29276601


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11089599 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:21569298 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13538238 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689710 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150544910 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10051549 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:23967202 PMID:25741868 PMID:28492532 PMID:30245029


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11094651 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610874 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:11139240 PMID:24033266 PMID:24416283 PMID:25333064 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155737246 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735307 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736773 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155724348 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735997 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736258 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155729654 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736580 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155737232 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155723998 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155724064 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155726140 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735993 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155726743 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792210 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24154662 PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11646883 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38498286 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558499 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:12702164 PMID:20142502 PMID:24033266 PMID:25262649 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690949 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784409 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:23251578 PMID:28492532 PMID:29490346


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903605 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906933 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783074 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24498627 PMID:25356976 PMID:25741868 PMID:28492532 PMID:33095980


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906945 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558496 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:11139240 PMID:17407589 PMID:20301442 PMID:20671281 PMID:21203349 PMID:25560255 PMID:25741868 PMID:27440999 PMID:27957503 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689708 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558498 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:12136232 PMID:16963483 PMID:24033266 PMID:24875298 PMID:25741868 PMID:28492532 PMID:29739340


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610860 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13435426 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:28041643 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906935 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903606 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610867 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906942 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602605 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906928 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38458612 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792381 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905925 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906932 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610887 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150413628 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785358 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:27460420 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783164 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:12107438 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25525159 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690831 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786669 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:16199547 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28909692 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693563 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614720 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784819 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790253 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:21487335 PMID:22135276 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11096420 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610884 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610891 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789567 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:22135276 PMID:25788563 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906931 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788650 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11643946 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610840 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38458605 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13537375 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:17576681 PMID:24033266 PMID:28492532 PMID:9536098


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13526319 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:17576681 PMID:24033266 PMID:28492532 PMID:9536098


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Ush1c (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: OMIM:276904


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12738711 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:11139240 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:22135276 PMID:24416283 PMID:24498627 PMID:25525159 PMID:25741868 PMID:27743452 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784773 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:27957503 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782515 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:12107438 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782775 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790506 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532 PMID:29625443


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784487 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12738845 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25356976 PMID:25468891 PMID:25525159 PMID:25741868 PMID:27460420 PMID:28492532 PMID:30303587


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782631 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783798 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:25741868


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790782 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782734 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558490 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:16199547 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532 PMID:9760205


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785929 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12905460 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:10973247 PMID:17407589 PMID:20301442 PMID:21203349 PMID:25741868 PMID:28492532 PMID:32531858


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610859 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:23967202 PMID:24033266 PMID:28492532 PMID:30311386 PMID:32036094 PMID:34148116


  • An association has been curated linking USH1C and Usher syndrome type 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28909583 (Homo sapiens)
  • 1 RGD objects have been annotated to Usher syndrome type 1C  (DOID:0110830)
  • 17 papers in RGD have been used to annotate USH1C
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1C
  • Original References(s): PMID:28492532


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