NIPA1 Polyclonal Antibody, 100ul Plasma Mutations of this gene result

Mutations of this gene result in factor X deficiency

The expression of this gene appears to be restricted to spermatocytes

A pseudogene of SLC9A7 is found on chromosome 12

LAG-1 (CSL) with ICN

The alpha chain is approximately 33-35 kDa

NIPA1 Polyclonal Antibody, 100ul Plasma Mutations of this gene resultThis 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.