基因注释：SLC17A8
官方信息
官方名称：solute carrier family 17 member 8
功能摘要：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].
作为靶基因的剪接因子
关联疾病
该基因暂无关联疾病记录