CLCN2 Polyclonal Antibody, 100ul Enzyme-Linked Immunosorbent Assay (ELISA) Mutations in this gene are

Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia

In addition| protein levels decrease in the presence of natural killer lytic-associated molecule| suggesting that association with natural killer lytic-associated molecule results in ubiquitination and subsequent degradation of this protein

The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36

a fibronectin-like motif

CLCN2 Polyclonal Antibody, 100ul Enzyme-Linked Immunosorbent Assay (ELISA) Mutations in this gene areThis gene encodes a voltage gated chloride channel. The encoded protein is a transmembrane protein that maintains chloride ion homeostasis in various cells. Defects in this gene may be a cause of certain epilepsies. Four transcript variants encoding different isoforms have been found for this gene.