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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking MECP2 and Rett syndrome in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • The annotation has been inferred from sequence orthology with Mecp2 (Rattus norvegicus) [(IMP) inferred from mutant phenotype]
  • 38 additional annotations were made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 36 RGD objects have been annotated to Rett syndrome  (DOID:1206)
  • 22 papers in RGD have been used to annotate MECP2


    • An association has been curated linking Mecp2 and Rett syndrome in Rattus norvegicus.        

  • The association was inferred from mutant phenotype (IMP)
    		•  
  • The annotation was made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 38 additional annotations were made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 36 RGD objects have been annotated to Rett syndrome  (DOID:1206)
  • 55 papers in RGD have been used to annotate Mecp2


    • An association has been curated linking Mecp2 and Rett syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • The annotation has been inferred from sequence orthology with Mecp2 (Rattus norvegicus) [(IMP) inferred from mutant phenotype]
  • 38 additional annotations were made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 36 RGD objects have been annotated to Rett syndrome  (DOID:1206)
  • 25 papers in RGD have been used to annotate Mecp2


    • An association has been curated linking Mecp2em1Sage and Rett syndrome in Rattus norvegicus.        

  • The association was inferred from mutant phenotype (IMP)
    		•  
  • The annotation was made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 38 additional annotations were made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 36 RGD objects have been annotated to Rett syndrome  (DOID:1206)
  • 4 papers in RGD have been used to annotate Mecp2em1Sage


    • An association has been curated linking SD-Mecp2em1Sage and Rett syndrome in Rattus norvegicus.        

  • The association was inferred from mutant phenotype (IMP)
    		•  
  • The annotation was made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 38 additional annotations were made from Wu Y, etal., J Neurodev Disord. 2016 Jun 16;8:23. doi: 10.1186/s11689-016-9156-7. eCollection 2016.
  • 36 RGD objects have been annotated to Rett syndrome  (DOID:1206)
  • 4 papers in RGD have been used to annotate SD-Mecp2em1Sage


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