FA69B Rabbit Polyclonal Antibody, 100ul Multiplex Immunoassays Mutations in this gene have

Mutations in this gene have been associated with the X-linked form of Opitz syndrome

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

interact with membrane-bound receptors

a major plasma protein produced by the yolk sac and the liver during fetal life

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FA69B Rabbit Polyclonal Antibody, 100ul Multiplex Immunoassays Mutations in this gene haveThis gene encodes a member of the FAM69 family of cysteine rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown.