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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking MSX2 and craniosynostosis in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Ma L, etal., Hum Mol Genet. 1996 Dec;5(12):1915-20.
  • 2 additional annotations were made from Ma L, etal., Hum Mol Genet. 1996 Dec;5(12):1915-20.
  • 466 RGD objects have been annotated to craniosynostosis  (DOID:2340)
  • 9 papers in RGD have been used to annotate MSX2
  • Curation Notes: craniosynostosis type 2, OMIM:604757, DNA:point mutation:exon:P148H


    • An association has been curated linking Msx2 and craniosynostosis in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Ma L, etal., Hum Mol Genet. 1996 Dec;5(12):1915-20.
  • 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 Ma L, etal., Hum Mol Genet. 1996 Dec;5(12):1915-20.
  • 466 RGD objects have been annotated to craniosynostosis  (DOID:2340)
  • 20 papers in RGD have been used to annotate Msx2
  • Curation Notes: craniosynostosis type 2, OMIM:604757, DNA:point mutation:exon:P148H


    • An association has been curated linking Msx2 and craniosynostosis in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Ma L, etal., Hum Mol Genet. 1996 Dec;5(12):1915-20.
  • 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 Ma L, etal., Hum Mol Genet. 1996 Dec;5(12):1915-20.
  • 466 RGD objects have been annotated to craniosynostosis  (DOID:2340)
  • 12 papers in RGD have been used to annotate Msx2
  • Curation Notes: craniosynostosis type 2, OMIM:604757, DNA:point mutation:exon:P148H


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