TRPM7 Polyclonal Antibody, 50ul Bio-Reaction Tube Mutations in this gene cause

Mutations in this gene cause familial juvenile nephronophthisis type 1

May be the cardiac P2Y receptor involved in the regulation of cardiac muscle contraction through modulation of L-type calcium currents

and it appears to regulate HER2

The CBC promotes pre-mRNA splicing

It also serves as cell surface receptor for the cytokine macrophage migration inhibitory factor (MIF) which

TRPM7 Polyclonal Antibody, 50ul Bio-Reaction Tube Mutations in this gene causeThe protein encoded by this gene is both an ion channel and a serine threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. Defects in this gene are a cause of amyotrophic lateral sclerosis parkinsonism dementia complex of Guam. Alternative splicing of this gene results in multiple transcript variants.