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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking FANCI 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:8566899 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 8 papers in RGD have been used to annotate FANCI
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:15477547 PMID:15689359 PMID:16177225 PMID:16621917 PMID:17088268 PMID:17426723 PMID:17438011 PMID:17950645 PMID:17980715 PMID:18991199 PMID:19010300 PMID:20691285 PMID:21038416 PMID:21228398 PMID:23783014 PMID:24033266 PMID:25462018 PMID:25741868 PMID:26104464 PMID:26467025 PMID:28492532


    • An association has been curated linking FANCI 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:8566903 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 8 papers in RGD have been used to annotate FANCI
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking FANCI 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:156319614 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 8 papers in RGD have been used to annotate FANCI
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


    • An association has been curated linking FANCI 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:126919679|RGD:14737585|RGD:15130250|RGD:156303754|RGD:26902416 (Homo sapiens) & RGD:126919679|RGD:14737585|RGD:15130250|RGD:156303754|RGD:26902416 (Homo sapiens) & RGD:126919679|RGD:14737585|RGD:15130250|RGD:156303754|RGD:26902416 (Homo sapiens) & RGD:126919679|RGD:14737585|RGD:15130250|RGD:156303754|RGD:26902416 (Homo sapiens) & RGD:126919679|RGD:14737585|RGD:15130250|RGD:156303754|RGD:26902416 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 8 papers in RGD have been used to annotate FANCI
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking FANCI 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:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens) & RGD:13214874|RGD:13482849|RGD:13814298|RGD:151716688|RGD:151808204|RGD:151882336|RGD:152061665|RGD:28885106|RGD:38499496 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 8 papers in RGD have been used to annotate FANCI
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FANCI 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:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens) & RGD:156021562|RGD:156069047|RGD:156076610|RGD:156111954|RGD:156158352|RGD:156191902|RGD:156276799|RGD:156356835|RGD:329371729|RGD:329391922|RGD:401724190|RGD:401737980|RGD:401739202 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 8 papers in RGD have been used to annotate FANCI
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking FANCI 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:8660404|RGD:8692501 (Homo sapiens) & RGD:8660404|RGD:8692501 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 8 papers in RGD have been used to annotate FANCI
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


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