靶标：
CLN5
产品别名：
CLN5； CLN5 intracellular trafficking protein； CLN5 intracellular trafficking protein； ceroid-lipofuscinosis neuronal protein 5； ceroid-lipofuscinosis, neuronal 5； 神经细胞蜡样质脂褐质沉积病蛋白CLN5；
背景信息：
ceroid-lipofuscinosis, neuronal 5(CLN5) Homo sapiens This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008],
