TRPM7 Polyclonal Antibody, 100ul Aspirating Pipets disease:Defects in STAT1 are a

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

and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage

Mutations in this gene are associated with mitochondriopathy and macrocytic anemia

|disease:A chromosomal aberration involving BCL6 may be a cause of lymphoma

The protein encoded by this gene is a member of the FPS/FES family of non-transmembrane receptor tyrosine kinases

TRPM7 Polyclonal Antibody, 100ul Aspirating Pipets disease:Defects in STAT1 are aThe 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.