SH3PXD2B wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SH3PXD2B wild-type allele is located in the vicinity of 5q35.1 and is approximately 129 kb in length. This allele, which encodes SH3 and PX domain-containing protein 2B, plays a role in podosome assembly. Mutation of the gene is associated with Frank-Ter Haar syndrome.

**Synonyms:** - FAD49 - FLJ20831 - FTHS - HOFI - KIAA1295 - SH3 and PX Domains 2B wt Allele - TKS4 - TSK4