×
![]()
- accession：NM_000441
- 基因别名：SLC26A4
- 基因描述：Homo sapiens solute carrier family 26 (anion exchanger), member 4 (SLC26A4), mRNA.
- 载体：现货载体
- CDS区长度：2343
- 翻译后氨基酸长度：780
- 基因简介：Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [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
