TRPM7 Polyclonal Antibody, 20ul Live Cell Imaging Mutations in this gene are

Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta

CYP20A1 (cytochrome P450 family 20 subfamily A member 1) encodes a member of the cytochrome P450 superfamily of enzymes

Mutations in NODAL are associated with heterotaxy

where it partially colocalizes with the nuclear lamina

TRPM7 Polyclonal Antibody, 20ul Live Cell Imaging 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.