SEMA6A wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SEMA6A wild-type allele is located in the vicinity of 5q23.1 and is approximately 131 kb in length. This allele, which encodes semaphorin-6A protein, is involved in cell-cell signaling and axon guidance in the developing central nervous system. Mutations in this gene are associated with both neuroaxonal dystrophy and mouth disease.

**Synonyms:** - HT018 - KIAA1368 - SEMA - SEMA6A-1 - SEMA6A1 - SEMAQ - Sema Domain, Transmembrane Domain (TM), and Cytoplasmic Domain, (Semaphorin) wt Allele - VIA