人 SLC17A8 (NM_001145288) cDNA克隆

Accession: NM_001145288
基因名称: SLC17A8
基因别名: DFNA25; VGLUT3
基因描述: Homo sapiens solute carrier family 17 (vesicular glutamate transporter), member 8 (SLC17A8), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1620 (查看编码区序列)
翻译后氨基酸长度: 539 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an exon in the coding region compared to variant 1. The encoded isoform (2) is shorter but has the same N- and C-termini compared to isoform 1.
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G123222 人 SLC17A8 (NM_001145288) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]