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GENE - TERM ANNOTATION REPORT

27 Annotations Found.

An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by OMIM:603358
  • Original References(s): PMID:12215968


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by OMIM:603358
  • Original References(s): PMID:19285991


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12910490 PMID:20727375 PMID:28322498 PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by OMIM:603358


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:11528392 PMID:12215968 PMID:12547234 PMID:18386115 PMID:19508421 PMID:21274865 PMID:25741868 PMID:25914718 PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:11528392 PMID:17314340 PMID:20518024 PMID:23892085 PMID:24655110 PMID:28492532 PMID:29090881


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:25895478 PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:28105683


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17403714 PMID:24033266


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:26489029


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17314340 PMID:17403714 PMID:27959697 PMID:28492532 PMID:30582773 PMID:31435670


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:28322498


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24236502 PMID:26489029


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12215968 PMID:22277166


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:19389488 PMID:28496993


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266 PMID:26467025


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17314340 PMID:17403714 PMID:20518024


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17403714 PMID:22310368


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:18771761 PMID:24033266 PMID:26467025


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12215968 PMID:17314340 PMID:25895478 PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12215968 PMID:12910490 PMID:19389488 PMID:19508421 PMID:20518024 PMID:22277166 PMID:25741868 PMID:28492532


  • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17314340 PMID:25741868 PMID:28492532


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