Skip to main content
. Author manuscript; available in PMC: 2018 Feb 1.
Published in final edited form as: Ann Neurol. 2017 Jan 27;81(2):227–239. doi: 10.1002/ana.24847

Figure 2. Scheme of FYCO1.

Figure 2

Black arrows denote sites of missense variants identified in patients with sIBM. Red arrows denote mutations previously identified in patients with congenital cataracts. Domains include RUN (GTPase interacting motif); Coiled Coil (dimerization motif); FYVE (phospholipid binding region); LIR (LC3 interacting region); and GOLD (golgi dynamics domain).