CD6 Polyclonal Antibody, 50ul[BT-AP02120] Gloves Mutations in this gene cause

Mutations in this gene cause autosomal recessive nonsyndromic deafness| type 18B

Interacts with ZNF289/ARFGAP2 through its C-terminal appendage domain

This protein is speculated to be involved in the cAMP-dependent signal transduction pathway and in directing RNA to a specific cellular compartment

has a vent cap

targeting these proteins for lysosome-dependent degradation

CD6 Polyclonal Antibody, 50ul[BT-AP02120] Gloves Mutations in this gene causeGJA5 is a member of the connexin gene family. The gap junction protein alpha 5 is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene may be associated with atrial fibrillation. Alternatively spliced transcript variants encoding the same isoform have been described.