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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking CLRN1-AS1 and Usher syndrome type 3A in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558072 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 3A  (DOID:0110841)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3A
  • Original References(s): PMID:12080385 PMID:12145752 PMID:14569126 PMID:16028794 PMID:18281613 PMID:19423712 PMID:19753315 PMID:22787034 PMID:24033266 PMID:25741868 PMID:26180195 PMID:28041643 PMID:28492532 PMID:34906470


    • An association has been curated linking CLRN1-AS1 and Usher syndrome type 3A in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611010 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 3A  (DOID:0110841)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3A
  • Original References(s): PMID:22135276 PMID:24033266 PMID:28492532


    • An association has been curated linking CLRN1-AS1 and Usher syndrome type 3A in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15169100 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 3A  (DOID:0110841)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3A
  • Original References(s): PMID:28492532


    • An association has been curated linking CLRN1-AS1 and Usher syndrome type 3A in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611011 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 3A  (DOID:0110841)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3A
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking CLRN1-AS1 and Usher syndrome type 3A in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8568440 (Homo sapiens)
  • 3 RGD objects have been annotated to Usher syndrome type 3A  (DOID:0110841)
  • 1 papers in RGD have been used to annotate CLRN1-AS1
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 3A
  • Original References(s): PMID:21310491 PMID:25741868


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