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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Chmp2b and Frontotemporal Lobar Degeneration in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Ghazi-Noori S, etal., Brain. 2012 Mar;135(Pt 3):819-32.
  • The annotation has been inferred from sequence orthology with CHMP2B (Homo sapiens) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Ghazi-Noori S, etal., Brain. 2012 Mar;135(Pt 3):819-32.
  • 172 RGD objects have been annotated to Frontotemporal Lobar Degeneration  (DOID:9002031)
  • 15 papers in RGD have been used to annotate Chmp2b


    • An association has been curated linking Chmp2b and Frontotemporal Lobar Degeneration in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Kaivorinne AL, etal., Eur J Neurol. 2010 Nov;17(11):1393-5.
  • The annotation has been inferred from sequence orthology with CHMP2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Kaivorinne AL, etal., Eur J Neurol. 2010 Nov;17(11):1393-5.
  • 172 RGD objects have been annotated to Frontotemporal Lobar Degeneration  (DOID:9002031)
  • 15 papers in RGD have been used to annotate Chmp2b
  • Qualifier: no_association


    • An association has been curated linking Chmp2b and Frontotemporal Lobar Degeneration 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 CHMP2B (Homo sapiens) [(EXP) inferred from experiment]
  • 172 RGD objects have been annotated to Frontotemporal Lobar Degeneration  (DOID:9002031)
  • 15 papers in RGD have been used to annotate Chmp2b
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:17956895


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