🧬 基因注释：SLITRK6
📝 官方信息
官方名称：SLIT and NTRK like family member 6
功能摘要：This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing and vision. Mutations in this gene are a cause of myopia and deafness. [provided by RefSeq, Dec 2014].
🏥 关联疾病
该基因暂无关联疾病记录