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- accession：NM_006996
- 基因别名：SLC19A2
- 基因描述：Homo sapiens solute carrier family 19 (thiamine transporter), member 2 (SLC19A2), mRNA.
- 载体：现货载体
- CDS区长度：1494
- 翻译后氨基酸长度：497
- 基因简介：This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. [provided by RefSeq, Jul 2008]
- 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
