TWNK FISH Probe

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]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
TWNK-20-RE 20 (40 μL) 200 μL color Request Pricing
TWNK-20-OR 20 (40 μL) 200 μL color Request Pricing
TWNK-20-GO 20 (40 μL) 200 μL color Request Pricing
TWNK-20-GR 20 (40 μL) 200 μL color Request Pricing
TWNK-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene 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]

Gene Details

Gene Symbol : TWNK

Gene Name : Twinkle mtDNA helicase

Chromosome : CHR 10: 100,987,526-100,994,402

Locus : 10q24.31

Alt. Genes : LRPPRC

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