AMPD1 Polyclonal Antibody, 100ul Bio-Reaction Tube Mutations in this gene have

Mutations in this gene have been linked to hyperparathyroidism-jaw tumor syndrome

may be a cause of multiple myeloma

Alternative splicing seems to be a common mechanism in this gene family

The sphingolipid metabolite sphingosine-1-phosphate promotes cell proliferation and survival

This gene encodes a member of the WD repeat protein family

AMPD1 Polyclonal Antibody, 100ul Bio-Reaction Tube Mutations in this gene haveAdenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver and erythocyte specific isoforms, respectively. Deficiency of the muscle specific enzyme is apparently a common cause of exercise induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively