MLXPL Rabbit Polyclonal Antibody, 20ul DNA Libraries Synthesis Mutations in this gene are

Mutations in this gene are associated with hypogonadotropic hypogonadism

There are two isoforms of this protein

antinociception

Mutations in APP have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy)

MLXPL Rabbit Polyclonal Antibody, 20ul DNA Libraries Synthesis Mutations in this gene areThis gene encodes a basic helix loop helix leucine zipper transcription factor of the Myc Max Mad superfamily. This protein forms a heterodimeric complex and binds and activates in a glucose dependent manner carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams Beuren syndrome a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11. 23.