NIPA1 Polyclonal Antibody, 20ul Digital Burette Mutations in this gene are

Mutations in this gene are associated with Schinzel-Giedion midface retraction syndrome

This gene encodes a member of the CRMP (collapsing response mediator protein) family thought to be involved in neural development

reducing the risk of contamination during handling

a secreted serine protease that converts the proenzyme plasminogen to plasmin

suggesting that the protein may suppress tumor invasion and metastasis

NIPA1 Polyclonal Antibody, 20ul Digital Burette 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.