- accession:NM_014270
- 基因别名:SLC7A9
- 基因描述:Homo sapiens solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 (SLC7A9), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1464
- 翻译后氨基酸长度:487
- TranscriptVariant:This variant (1) represents the longest transcript. Variants 1, 2, and 3 encode the same protein.
- 基因简介:This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq, Jul 2011]
- 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