PEX6 Polyclonal Antibody, 50ul Liquid Storage Consumables Mutations in KCNT1 cause the

Mutations in KCNT1 cause the early-onset epileptic disorders

A nucleolar staining may be due to nuclear targeting of an isoform lacking the transmembrane domain (By similarity)

globular and stalk domains

transcriptional regulation

PI4KII phosphorylates PtdIns at the D-4 position

PEX6 Polyclonal Antibody, 50ul Liquid Storage Consumables Mutations in KCNT1 cause theThis gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C terminal tripeptide of the sequence ser lys leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and