DPYSL5 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human DPYSL5 wild-type allele is located in the vicinity of 2p23.3 and is approximately 103 kb in length. This allele, which encodes dihydropyrimidinase-related protein 5, plays a role in the negative regulation of axon and dendrite morphogenesis. Mutation of the gene is associated with Ritscher-Schinzel syndrome 4.

**Synonyms:** - CRAM - CRMP-5 - CRMP5 - CV2 - Dihydropyrimidinase Like 5 wt Allele - Dihydropyrimidinase-Like 5 Gene - RTSC4 - ULIP6 - Ulip6