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SYNE1 gene

spectrin repeat containing nuclear envelope protein 1

Key facts

Official symbol
SYNE1
Full name
SYNE1
Chromosome
6
Map location
6q25.2
Organism
Homo sapiens
NCBI Gene ID
23345
Also known as
8B, AMC3, AMCM, ARCA1, C6orf98, CPG2

Function summary

This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008].

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Data source: NCBI Gene · alsesAI Gene Library