SYNE1 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human SYNE1 wild-type allele is located in the vicinity of 6q25.2 and is approximately 516 kb in length. This allele, which encodes nesprin-1 protein, is involved in the subcellular position of the nucleus. Mutation of the gene is associated with autosomal recessive spinocerebellar ataxia 8.
**Synonyms:** - 8B - ARCA1 - C6orf98 - CPG2 - CPG2 Full Length Gene - Chromosome 6 Open Reading Frame 98 Gene - EDMD4 - KASH1 - KIAA0796 - KIAA1262 - KIAA1756 - MYNE1 - Nesp1 - Nuclear Envelope Spectrin Repeat-1 Gene - SCAR8 - Spectrin Repeat Containing Nuclear Envelope Protein 1 wt Allele - Spectrin Repeat Containing, Nuclear Envelope 1 Gene - Synaptic Nuclei Expressed Gene 1 - dJ45H2.2
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Cross-system equivalences0
No cross-system equivalences mapped for this node.