FBLN2 (Fibulin 2) is a Protein Coding gene. Diseases associated with FBLN2 include Cutis Laxa and Brachyolmia Type 4 With Mild Epiphyseal And Metaphyseal Changes. Among its related pathways are Elastic fibre formation and Extracellular matrix organization. Gene Ontology (GO) annotations related to this gene include calcium ion binding and extracellular matrix binding. An important paralog of this gene is FBLN1.