- accession:NM_000084
- 基因别名:CLCN5
- 基因描述:Homo sapiens chloride channel, voltage-sensitive 5 (CLCN5), transcript variant 3, mRNA.
- 载体: 现货载体
- CDS区长度:2241
- 翻译后氨基酸长度:746
- TranscriptVariant:This variant (3, also known as type 3) lacks several 5' exons but has an alternate 5' exon, and it thus differs in the 5' UTR and uses a downstream start codon, compared to variant 1. The resulting isoform (b) has a shorter N-terminus, compared to isoform a.
- 基因简介:This gene encodes a member of the ClC family of chloride ion channels and ion transporters. The encoded protein is primarily localized to endosomal membranes and may function to facilitate albumin uptake by the renal proximal tubule. Mutations in this gene have been found in Dent disease and renal tubular disorders complicated by nephrolithiasis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]
- 载体信息:自有图片地址
- 规格:10ul 质粒
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