靶标：
MID1
产品别名：
BBBG1； FXY； GBBB； GBBB1； MIDIN； OGS1； OS； OSX； RNF59； TRIM18； XPRF； ZNFXY； MID1； midline 1； midline 1； E3 ubiquitin-protein ligase Midline-1； Opitz/BBB syndrome； RING finger protein 59； RING finger protein Midline-1； RING-type E3 ubiquitin transferase Midline-1； midline 1 RING finger protein； putative transcription factor XPRF； tripartite motif protein TRIM18； tripartite motif-containing protein 18； zinc finger on X and Y, mouse, homolog of； Midline 1蛋白(MID1)； 环指蛋白59；
背景信息：
midline 1(MID1) Homo sapiens The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Multiple different transcript variants are generated by alternate splicing; however, t
