CPXCR Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing Mutations in this gene are

Mutations in this gene are associated with progressive epilepsy with mental retardation (EMPR)

and at lower levels in skeletal muscle

AMIGO family

Sulfotransferases aid in the metabolism of drugs and endogenous compounds by converting these substances into more hydrophilic water-soluble sulfate conjugates that can be easily excreted

and plays a regulatory role in Fas-mediated apoptosis

CPXCR Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing Mutations in this gene areThis gene is one of several genes identified in a region of the X chromosome associated with an X linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified.