VEZF1 Polyclonal Antibody, 20ul Centrifugal Filter Various mutations of PMP22 are

Various mutations of PMP22 are causes of Charcot-Marie-Tooth disease Type IA

PTM:Phosphorylated by GRK6 upon leukotriene B4 binding

Alternatively spliced transcript variants encoding different isoforms have been found for IL18R1

targeting these proteins for lysosome-dependent degradation

This gene encodes a member of the WWC family of proteins| which also includes the WWC1 (KIBRA) gene product and the WWC2 gene product

VEZF1 Polyclonal Antibody, 20ul Centrifugal Filter Various mutations of PMP22 areTranscriptional regulatory proteins containing tandemly repeated zinc finger domains are thought to be involved in both normal and abnormal cellular proliferation and differentiation. ZNF161 is a C2H2 type zinc finger protein (Koyano Nakagawa et al., 1994