“…Functional TRP channels are either homo-or heterotetramers assembled from identical or similar TRP subunits [109,110]. Although evidences for hereditary channelopathies (e.g., mutations in the channel gene are essential for the pathogenesis of the disease and cause altered channel functions) have only been described for few TRP family members, emerging genetic analysis data identify most of Trp genes as potential risk factors for many disease states [1,2,13,59,64,101,104]. Importantly, associations between TRPs and diseases spot these channels as novel pharmaceutical targets (see [77,107,113,143]).…”