SNX29 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SNX29 wild-type allele is located in the vicinity of 16p13.13 and is approximately 598 kb in length. This allele, which encodes sorting nexin-29 protein, may play a role in the regulation of GTPase-mediated signaling or lipid trafficking. A point mutation in the gene may be associated with ovarian serous carcinoma.

**Synonyms:** - A-388D4.1 - FLJ12363 - RUN Domain Containing 2A Gene - RUNDC2 - RUNDC2A - Sorting Nexin 29 wt Allele