RAB39B wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human RAB39B wild-type allele is located in the vicinity of Xq28 and is approximately 6 kb in length. This allele, which encodes Ras-related protein Rab-39B, plays a role in the localization of proteins involved in synaptic transmission and autophagy. Mutations in the gene are associated with Waisman syndrome and X-linked intellectual developmental disorder 72.

**Synonyms:** - BGMR - MRX72 - Mental Retardation, X-Linked 72 Gene - RAB39B, Member RAS Oncogene Family wt Allele - WSMN - WSN - Waisman Syndrome Gene - XLID72