Mine Disruption Phenotype

Gene Info

  • Species:Mouse (Mus musculus)
  • GeneID:14119
  • Symbol:Fbn2
  • Description:fibrillin 2
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Gene ID Entry Entry Name Protein Name Type Information
14119 Q61555 FBN2_MOUSE Fibrillin-2 [Cleaved into: Placensin] DISRUPTION PHENOTYPE Limb-patterning defects characterized by bilateral syndactyly due to disorganized matrix (PubMed:11470817). Digit fusion involves both soft and hard tissues and is associated with reduced apoptosis at affected sites (PubMed:11470817). Mice show a well developed and morphologically normal aortic wall (PubMed:16407178). Mice display a low bone mass phenotype that is associated with reduced bone formation (PubMed:20855508). {ECO:0000269|PubMed:11470817, ECO:0000269|PubMed:16407178, ECO:0000269|PubMed:20855508}.