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

Mutations in TJP2 have been identified in patients with hypercholanemia

is a 786 amino acid protein containing one VIT domain and one VWFA domain

The encoded protein is thought to be a part of the semaphorin signal transduction pathway implicated in semaphorin-induced growth cone collapse during neural development

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

This gene encodes a protein that belongs to the Mig10/Rap1-interacting adaptor molecule/Lamellipodin family of adapter proteins

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