NHE-6 Polyclonal Antibody, 100ul RNA Tools and mutations in this gene

and mutations in this gene may play a role in amyotrophic lateral sclerosis

Phospholipid scramblases are membrane proteins that mediate calcium-dependent

ALK/KIF5B (chromosome 10)

a disease characterized by recurrent bacterial infections

Paired amphipathic helix protein Sin3b acts as a transcriptional repressor

NHE-6 Polyclonal Antibody, 100ul RNA Tools and mutations in this geneSLC9A6 encodes a sodium hydrogen exchanger that is amember of the solute carrier family 9. The solute carrier family 9 member A6 localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X linked syndromic mental retardation, Christianson type. Alternate splicing results in multiple transcript variants.