PLXNC1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human PLXNC1 wild-type allele is located in the vicinity of 12q23.3 and is approximately 159 kb in length. This allele, which encodes plexin-C1 protein, plays a role in semaphorin-dependent signaling leading to cytoskeletal remodeling.

**Synonyms:** - CD232 - PLXN-C1 - Plexin C1 wt Allele - VESPR