ATL1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human ATL1 wild-type allele is located in the vicinity of 14q22.1 and is approximately 102 kb in length. This allele, which encodes atlastin-1 protein, plays a role in organization of the endoplasmic reticulum and axonal maintenance. Mutation of the gene is associated with hereditary sensory neuropathy 1D and autosomal dominant spastic paraplegia 3A.

**Synonyms:** - AD-FSP - Atlastin 1 Gene - Atlastin GTPase 1 wt Allele - Atlastin Gene - FSP1 - GBP3 - HSN1D - SPG3 - SPG3A - Spastic Paraplegia 3A (Autosomal Dominant) Gene - atlastin1