disease:Defects in CLN6 are the cause of variant late-onset infantile neuronal ceroid lipofuscinosis (vLINCL) [MIM:601780].,online information:Neural Ceroid Lipofuscinoses mutation db,
Endoplasmic reticulum membrane ; Multi-pass membrane protein . Endoplasmic reticulum .
Epithelium,Lung,Urinary bladder,