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WRN, WRN RecQ like helicase

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WRN, WRN RecQ like helicase

  • This gene encodes a member of the RecQ subfamily of DNA helicase proteins. The encoded nuclear protein is important in the maintenance of genome stability and plays a role in DNA repair, replication, transcription and telomere maintenance. This protein contains a N-terminal 3' to 5' exonuclease domain, an ATP-dependent helicase domain and RQC (RecQ helicase conserved region) domain in its central region, and a C-terminal HRDC (helicase RNase D C-terminal) domain and nuclear localization signal. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by accelerated aging and an elevated risk for certain cancers. [provided by RefSeq, Aug 2017]

  • Gene Synonyms (Werner syndrome ATP-dependent helicase, DNA helicase, RecQ-like type 3, Werner syndrome RecQ like helicase, Werner syndrome, RecQ helicase-like, exonuclease WRN, recQ protein-like 2, RECQ3, RECQL2, RECQL3,)
  • NCBI Gene ID: 7486
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q14191
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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