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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:12529855


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:12630957


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:12567411


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:12630957 PMID:18372316


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:11468277


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:12400065 PMID:16219626


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:11175783


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FOXL2 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:16219626 PMID:20429427 PMID:21889601


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:17089161


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:11468277 PMID:12529855 PMID:25741868


  • An association has been curated linking Foxl2 and Blepharophimosis Syndrome Type 1 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 FOXL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 8 papers in RGD have been used to annotate Foxl2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:11175783 PMID:11776388 PMID:12938087 PMID:25741868


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