fbn-1 [Browse genome (BioProject PRJNA13758)] [Legacy GBrowse]
Is predicted to have calcium ion binding activity. Is used to study connective tissue disease. Human ortholog(s) of this gene are implicated in autosomal recessive cutis laxa type IC and congenital contractural arachnodactyly. Is an ortholog of human FBN2 (fibrillin 2).