基因名：
Tctn2
产品别名：
4432405B04Rik； Tect2； Tctn2； tectonic family member 2； tectonic family member 2； tectonic-2； 结构蛋白家族2；
背景信息：
Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.
