- accession:NM_001042432
- 基因别名:CLN3
- 基因描述:Homo sapiens ceroid-lipofuscinosis, neuronal 3 (CLN3), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1317
- 翻译后氨基酸长度:438
- TranscriptVariant:This variant (1) represents the longest transcript. Both variants 1 and 2 encode the same isoform (a).
- 基因简介:This gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]
- 载体信息:自有图片地址
- 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