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GENE - TERM ANNOTATION REPORT

27 Annotations Found.

An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Dorsman JC, etal., Cell Oncol. 2007;29(3):211-8.
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Dorsman JC, etal., Cell Oncol. 2007;29(3):211-8.
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: DNA:mutations:exon, intron:multiple


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:17452773 PMID:17460694


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:17452773 PMID:25741868


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by OMIM:609053
  • Original References(s): PMID:17452773


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by OMIM:609053
  • Original References(s): PMID:17412408 PMID:17452773


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:22720145 PMID:24989076 PMID:26590883 PMID:28492532


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:28492532 PMID:28678401


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:25741868 PMID:26590883 PMID:28492532


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:28492532 PMID:28878254


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:25741868


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:17460694 PMID:17924555 PMID:21324748


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:28492532


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:18931676


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26296701 PMID:28492532 PMID:29439820


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:23613520


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:22778927


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:17460694


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:23093618


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:17452773 PMID:23613520 PMID:25741868 PMID:28492532


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:28492532 PMID:30076350


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:23524600 PMID:25741868 PMID:26467025 PMID:27987238 PMID:28492532


  • An association has been curated linking Fanci and Fanconi anemia complementation group I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCI (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Fanconi anemia complementation group I  (DOID:0111091)
  • 8 papers in RGD have been used to annotate Fanci
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group I
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28678401 PMID:30303537


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