×
![]()
- accession：NM_006493
- 基因别名：CLN5
- 基因描述：Homo sapiens ceroid-lipofuscinosis, neuronal 5 (CLN5), mRNA.
- 载体：现货载体
- CDS区长度：1224
- 翻译后氨基酸长度：407
- 基因简介：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]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
