PEG3 Polyclonal Antibody, 100ul Cell Culture Dishes Mutations in this gene have

Mutations in this gene have been associated with hypokalemic periodic paralysis

This family member functions in the translocation of peptides from the cytosol into the lysosomal lumen

nucleotide excision repair protein encoded by RAD23B is one of two human homologs of Saccharomyces cerevisiae Rad23

Mutations in this gene have also been associated with breast tumor development

The result of these interactions is regulation of cell motility

PEG3 Polyclonal Antibody, 100ul Cell Culture Dishes Mutations in this gene haveIn human, ZIM2 and PEG3 are treated as two distinct genes though they share multiple 5' exons and a common promoter and both genes are paternally expressed (PMID: 15203203). Alternative splicing events connect their shared 5' exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. In contrast, in other mammals ZIM2 does not undergo imprinting and, in mouse, cow, and likely other mammals as well, the ZIM2