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 |
|---|---|---|---|---|
| CLN5-20-RE | 20 (40 μL) | 200 μL |  |
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| CLN5-20-OR | 20 (40 μL) | 200 μL |  |
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| CLN5-20-GO | 20 (40 μL) | 200 μL |  |
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| CLN5-20-GR | 20 (40 μL) | 200 μL |  |
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| CLN5-20-AQ | 20 (40 μL) | 200 μL |  |
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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 : CLN5
Gene Name : CLN5, intracellular trafficking protein
Chromosome : CHR 13: 769,919,23-770,025,16
Locus : 13q22.3
Alt. Genes : FEM1B
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