菜单 基因医生

这个基因编码一个btb-kelch超家族成员。最初被描述为一种基于与碱性亮氨酸拉链样家族成员弱同源性的假定转录调节器,随后编码的蛋白质被证明仅局限于高尔基网络,在那里它可能有助于稳定高尔基复合体。该基因缺失可能与Digeorge综合征有关。
This gene encodes a member of the BTB-kelch superfamily. Initially described as a putative transcriptional regulator based on weak homology to members of the basic leucine zipper-like family, the encoded protein subsequently has been shown to localize exclusively to the Golgi network where it may help stabilize the Gogli complex. Deletion of this gene may be associated with DiGeorge syndrome.

基因名:LZTR1
别名:BTBD29,LZTR-1,NS10,SWNTS2
基因ID:8216
Chromosome:
(GRCh37)
22 Start: 21333751 End: 21353327 Strand: 1
信号通路: 基因组不稳定 
LZTR1 基因突变与药物