PTPZeta Polyclonal Antibody, 50ul Aspirating Pipets Mutations in this gene are

Mutations in this gene are the cause of autosomal dominant Robinow syndrome

This gene is located on the long arm of chromosome 13

This gene encodes a full transporter and member of the p-glycoprotein family of membrane proteins with phosphatidylcholine as its substrate

HECT domain E3 ubiquitin ligases transfer ubiquitin from E2 ubiquitin-conjugating enzymes to protein substrates

The protein encoded by PEX11G (peroxisomal biogenesis factor 11 gamma) is a member of the PEX11 family

PTPZeta Polyclonal Antibody, 50ul Aspirating Pipets Mutations in this gene arePTPRZ1 encodes a member of the receptor protein tyrosine phosphatase family. Expression of PTPRZ1 is restricted to the central nervous system (CNS), and it may be involved in the regulation of specific developmental processes in the CNS. Alternatively spliced transcript variants encoding different isoforms have been described for PTPRZ1.