FIGURE 15.
TRPC6 mutations associated with familial focal segmental glomerulosclerosis (FSGS). Domain structure of the TRPC6 channel. Human mutations associated with FSGS are shown in boxes. All of the known disease-causing mutations are located in the amino- and carboxy-terminal portions of TRPC6 that extend into the cytosol. Adapted from Ref. 349 with permission.