MID1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human MID1 wild-type allele is located in the vicinity of Xp22.2 and is approximately 388 kb in length. This allele, which encodes E3 ubiquitin-protein ligase Midline-1 protein, plays a role in the modulation of microtubule organization. Mutations in this gene may be associated with the X-linked form of Opitz syndrome.

**Synonyms:** - BBBG1 - FXY - Finger on X and Y, Mouse, Homolog of Gene - GBBB1 - MIDIN - Midline 1 (Opitz/BBB Syndrome) Gene - Midline 1 RING Finger Gene - Midline 1 wt Allele - OGS1 - OS - OSX - RNF59 - TRIM18 - XPRF - ZNFXY - Zinc Finger on X and Y, Mouse, Homolog of Gene