NIPA1 Polyclonal Antibody, 50ul Centrifuges Mutations in this gene are

Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia

whereby some individuals have a functional allele that encodes a full-length protein

encephalomyopathies

This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region

developmental stage:Expressed in early stage of myeloid and erythroid differentiation

NIPA1 Polyclonal Antibody, 50ul Centrifuges Mutations in this gene areThis gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6.