MRP Polyclonal Antibody, 20ul Pathway and Network Analysis Mutations in PKD2 are associated

Mutations in PKD2 are associated with autosomal dominant polycystic kidney disease type 2

neurophysin 2 and copeptin

The p-TEFb complex containing this cyclin was reported to interact with

thyrotoxic periodic paralysis and malignant hyperthermia susceptibility

With a risk-taking attitude

MRP Polyclonal Antibody, 20ul Pathway and Network Analysis Mutations in PKD2 are associatedThis gene encodes a member of the myristoylated alanine rich C kinase substrate (MARCKS) family. Members of this family play a role in cytoskeletal regulation, protein kinase C signaling and calmodulin signaling. The encoded protein affects the formation of adherens junction. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are located on the long arm of chromosomes 6 and 10.