TRPM7 Polyclonal Antibody, 100ul Aspirating Pipets Mutations in this gene are

Mutations in this gene are associated with mitochondriopathy and macrocytic anemia

disease:Defects in STAT1 are a cause of mendelian susceptibility to mycobacterial disease (MSMD)

Alternatively spliced transcript variants encoding different isoforms have been noted for DNAI2

which is a precursor to melanin synthesis

The protein encoded by KCNJ9 is an integral membrane protein and inward-rectifier type potassium channel

TRPM7 Polyclonal Antibody, 100ul Aspirating Pipets Mutations in this gene areThe 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.