人 SLC7A9 (NM_014270) cDNA克隆

Accession: NM_014270
基因名称: SLC7A9
基因别名: BAT1; CSNU3
基因描述: Homo sapiens solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 (SLC7A9), transcript variant 1, mRNA.
种属: Human
CDS区长度: 1464 (查看编码区序列)
翻译后氨基酸长度: 487 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the longest transcript. Variants 1, 2, and 3 encode the same protein.
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G119054 人 SLC7A9 (NM_014270) cDNA克隆 pDONR223 2ug质粒 点击询价

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]