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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CLN6-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| CLN6-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| CLN6-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| CLN6-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| CLN6-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
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]
Gene Symbol : CLN6
Gene Name : CLN6, transmembrane ER protein
Chromosome : CHR 15: 682,297,41-682,069,91
Locus : 15q23
Alt. Genes : OPTN
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.