VGLL1 Rabbit Polyclonal Antibody, 20ul Buffers & Solutions Mutations in this gene have

Mutations in this gene have been found in some patients with the CHARGE syndrome

and can be stored at 2-8℃ for maximum stability

Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G

controlling the alpha-1 subunit membrane targeting and shifting the voltage dependence of activation and inactivation

|Contains 1 SH2 domain

VGLL1 Rabbit Polyclonal Antibody, 20ul Buffers & Solutions Mutations in this gene haveThe protein encoded by this gene binds proteins of the TEA domain family of transcription factors (TEFs) through the Vg (vestigial) homology region found in its N terminus. It may thus function as a specific coactivator for the mammalian TEFs.