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

the cellular RAF1 protein can phosphorylate to activate the dual specificity protein kinases MEK1 and MEK2

May promote HRAS-mediated transformation

The encoded protein may play a role in multiple cellular processes by regulating the MAP kinase

1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor

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.