Mine Disruption Phenotype

Gene Info

  • Species:Mouse (Mus musculus)
  • GeneID:17286
  • Symbol:Meox2
  • Description:mesenchyme homeobox 2
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Gene ID Entry Entry Name Protein Name Type Information
17286 P32443 MEOX2_MOUSE Homeobox protein MOX-2 (Growth arrest-specific homeobox) (Mesenchyme homeobox 2) DISRUPTION PHENOTYPE Mice display defective differentiation and morphogenesis of the limb muscles, characterized by an overall reduction in muscle mass and elimination of specific muscles (PubMed:10403250, PubMed:12925591). Embryos also display a cleft palate phenotype at 15.5 dpc (PubMed:16284941). Mice lacking Meox1 and Meox2 show extremely disrupted somite morphogenesis, patterning and differentiation (PubMed:12925591). They lack an axial skeleton and skeletal muscles are severely deficient (PubMed:12925591). {ECO:0000269|PubMed:10403250, ECO:0000269|PubMed:12925591, ECO:0000269|PubMed:16284941}.