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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking CNGB3 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13532115 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:15657609 PMID:26106334


    • An association has been curated linking CNGB3 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens) & RGD:11638053|RGD:12743026|RGD:13515662|RGD:151751178|RGD:151805510|RGD:151834424|RGD:155934693|RGD:156019957|RGD:156100216|RGD:156265795|RGD:26885879|RGD:26890596|RGD:26904668|RGD:26914295|RGD:26915634|RGD:28868149 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking CNGB3 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens) & RGD:156082986|RGD:156105193|RGD:156141353|RGD:156202232|RGD:156260271|RGD:156286345|RGD:28907132|RGD:329359820|RGD:401765969 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking CNGB3 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151752263|RGD:38467085 (Homo sapiens) & RGD:151752263|RGD:38467085 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


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