FBLN1 and Syndactyly type 2: The fibulin-1 gene, which encodes both an extracellular matrix protein and a secreted plasma glycoprotein, has been found to be disrupted in a chromosomal translocation (12;22) which results in haploinsufficiency for the FBLN1-D variant in synpolydactyly, a congenital condition characterized by a union of fingers or toes and/or increase in the number of toes or fingers.