人 BSND (NM_057176) cDNA克隆

Accession: NM_057176
基因名称: BSND
基因别名: BART; DFNB73
基因描述: Homo sapiens Bartter syndrome, infantile, with sensorineural deafness (Barttin) (BSND), mRNA.
种属: Human
CDS区长度: 963 (查看编码区序列)
翻译后氨基酸长度: 320 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G119491 人 BSND (NM_057176) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes an essential beta subunit for CLC chloride channels. These heteromeric channels localize to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. Mutations in this gene have been associated with Bartter syndrome with sensorineural deafness. [provided by RefSeq, Jul 2008]