MAGE2 Polyclonal Antibody, 20ul Gloves Defects in this gene are

Defects in this gene are a cause of maturity-onset diabetes of the young type 7 (MODY7)

and contributes to T cell activation

the protein induces the rapid onset of crypt cell proliferation and increases intestinal epithelial healing

Mutations in this gene have been observed in individuals with amyotrophic lateral sclerosis 20

GO annotations related to this gene include oxidoreductase activity and cytochrome-b5 reductase activity

MAGE2 Polyclonal Antibody, 20ul Gloves Defects in this gene areThis gene encodes a member of the E subfamily of MAGE (melanoma antigen encoding gene) gene family. The gene is intronless and the encoded protein has two of the MAGE domains which are characteristic of MAGE family proteins.