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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking FOXL2 and Blepharophimosis Syndrome Type 1 in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596600 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8558322 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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


  • An association has been curated linking FOXL2 and Blepharophimosis Syndrome Type 1 in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8558317 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with FOXL2 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596603 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8558325 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8558323 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596602 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596598 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8558319 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596601 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD 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 Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8558316 (Homo sapiens)
  • 1 CRRD objects have been annotated to Blepharophimosis Syndrome Type 1  (DOID:9003489)
  • 0 papers in CRRD have been used to annotate FOXL2
  • Curation Notes: ClinVar Annotator: match by term: Blepharophimosis syndrome type 1
  • Original References(s): PMID:11468277


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.