SRGP1 Rabbit Polyclonal Antibody, 50ul Vacuum Aspirator Mutations in this gene have

Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome

This subunit forms a receptor complex with IL4 receptor alpha

and axonal and motor-sensory defects with deafness and mental retardation

Multiple alternatively spliced transcript variants encoding two isoforms with different length have been identified

SRGP1 Rabbit Polyclonal Antibody, 50ul Vacuum Aspirator Mutations in this gene haveThe protein encoded by this gene is a GTPase activator working with the GTPase CDC42 to negatively regulate neuronal migration. The encoded protein interacts with the transmembrane receptor ROBO1 to inactivate CDC42.