🧬 基因注释：SLC26A4
📝 官方信息
官方名称：solute carrier family 26 member 4
功能摘要：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].
🏥 关联疾病
该基因暂无关联疾病记录