DVL1 Polyclonal Antibody, 50ul Mini dry bath Mutations in TJP2 have been

Mutations in TJP2 have been identified in patients with hypercholanemia

Mutations in this gene cause autoimmune susceptibility 1

and is thought to be specifically chemotactic for T cells

some Ca(2+) also enters the cell through the sarcolemma (plasma membrane)

HIV-1 Tat protein was found to interact with this protein and cyclin T

DVL1 Polyclonal Antibody, 50ul Mini dry bath Mutations in TJP2 have beenDVL1, the human homolog of the Drosophila dishevelled gene (dsh) encodes a cytoplasmic phosphoprotein that regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. DVL1 is a candidate gene for neuroblastomatous transformation. The Schwartz Jampel syndrome and Charcot Marie Tooth disease type 2A have been mapped to the same region as DVL1. The phenotypes of these