FGF-16 Polyclonal Antibody, 50ul Bio-Reaction Tube Defects in this gene are

Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease

restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo

and the Golgi complex

and immune dysregulation syndrome and familial cold autoinflammatory syndrome 3

FGF-16 Polyclonal Antibody, 50ul Bio-Reaction Tube Defects in this gene areFGF16 encodes a member of a family of proteins that are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene is expressed in cardiac cells and is required for proper heart development. Mutation in this gene was also observed in individuals with metacarpal 4 5 fusion.