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TWNK gene

twinkle mtDNA helicase

Key facts

Official symbol
TWNK
Full name
TWNK
Chromosome
10
Map location
10q24.31
Organism
Homo sapiens
NCBI Gene ID
56652
Also known as
ATXN8, C10orf2, IOSCA, MTDPS7, PEO, PEO1

Function summary

This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009].

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Data source: NCBI Gene · alsesAI Gene Library