人 SLC26A5 (NM_206884) cDNA克隆

Accession: NM_206884
基因名称: SLC26A5
基因别名: PRES; DFNB61
基因描述: Homo sapiens solute carrier family 26 (anion exchanger), member 5 (SLC26A5), transcript variant c, mRNA.
种属: Human
CDS区长度: 1551 (查看编码区序列)
翻译后氨基酸长度: 516 (查看氨基酸序列)
Transcript Variant: This variant (c), also known as SLC26A5c, lacks multiple exons within the coding region and uses an alternate 3' end-exon compared to variant a. The resulting isoform (c) has a distinct and shorter C-terminus, as compared to isoform a.
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G123613 人 SLC26A5 (NM_206884) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]