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- accession：NM_033409
- 基因别名：SLC52A3
- 基因描述：Homo sapiens solute carrier family 52 (riboflavin transporter), member 3 (SLC52A3), mRNA.
- 载体：现货载体
- CDS区长度：1410
- 翻译后氨基酸长度：469
- 基因简介：This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]
- 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
