Chloride Channels are a superfamily of poorly understood ion channels specific for chloride. Though the functions of CLC cytoplasmic domains are not fully characterized yet, their importance is illustrated by the pathologies resulting from their mutations.

Voltage-gated chloride channels display a variety of important physiological and cellular roles that include regulation of pH, volume homeostasis, organic solute transport, cell migration, cell proliferation and differentiation. Based on sequence homology the chloride channels can be subdivided into a number of groups.

Mutations of CLCN2 causes following genetic disorders:

• Thomsen's disease
• Dent's disease
• Infantile malignantosteopetrosis
• Bartter's syndrome

Creative Bioarray offers access to screening services for multiple chloride channel targets.

Related Section

• Sodium Channels
• Calcium Channels
• Potassium Channels
• TRP Channels
• ATP gated P2X Channels
• ASICs
• Nicotinic Acetylcholine Receptors
• Ionotropic Glutamate-gated Receptors
• GABAa Receptors
• Glycine Receptors
• 5-HT Receptors3
• Cystic Fibrosis Transmembrane Conductance Regulators (CFTR)
• Other Ion Channels