TRPM7 Polyclonal Antibody, 100ul Aspirating Pipets |disease:A chromosomal aberration involving BCL6

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

Mutations in this gene are associated with mitochondriopathy and macrocytic anemia

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

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

TRPM7 Polyclonal Antibody, 100ul Aspirating Pipets |disease:A chromosomal aberration involving BCL6The 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.