SPG7 Polyclonal Antibody, 20ul Primary Antibodies Mutations in this gene are

Mutations in this gene are a cause of type 2E pseudohypoaldosteronism

referred to as a variable number tandem repeat or VNTR

Some individuals

X-linked 3) encodes a member of the ALEX family of proteins which may play a role in tumor suppression

SPG7 Polyclonal Antibody, 20ul Primary Antibodies Mutations in this gene areThis gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.