Mine Disruption Phenotype

Gene Info

  • Species:Mouse (Mus musculus)
  • GeneID:14118
  • Symbol:Fbn1
  • Description:fibrillin 1
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Gene ID Entry Entry Name Protein Name Type Information
14118 Q61554 FBN1_MOUSE Fibrillin-1 [Cleaved into: Asprosin] DISRUPTION PHENOTYPE Neonatal lethality due to ruptured aortic aneurysm, impaired pulmonary function and/or diaphragmatic collapse. Neonatal aorta show a disorganized and poorly developed medial layer but normal levels of elastin cross-links. {ECO:0000269|PubMed:16407178}.; DISRUPTION PHENOTYPE: [Asprosin]: Mice lacking Asprosin show low appetite, reduced adiposity and protection from diet-induced obesity. {ECO:0000269|PubMed:29106398}.