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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Msx2 and Craniofacial Abnormalities in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Wilkie AO, etal., Nat Genet. 2000 Apr;24(4):387-90.
  • The annotation has been inferred from sequence orthology with MSX2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Wilkie AO, etal., Nat Genet. 2000 Apr;24(4):387-90.
  • 2573 RGD objects have been annotated to Craniofacial Abnormalities  (DOID:9008731)
  • 20 papers in RGD have been used to annotate Msx2
  • Curation Notes: parietal foramina, OMIM:168500, DNA:point mutation:exon: R172H, DNA:deletions


    • An association has been curated linking Msx2 and Craniofacial Abnormalities 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 MSX2 (Homo sapiens) [(EXP) inferred from experiment]
  • 2573 RGD objects have been annotated to Craniofacial Abnormalities  (DOID:9008731)
  • 20 papers in RGD have been used to annotate Msx2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:9147639


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