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FLASH GENE
Symbol WRN contributors: mct/ - updated : 23-08-2019
HGNC name Werner syndrome, RecQ helicase-like
HGNC id 12791
ASSOCIATED DISORDERS
corresponding disease(s) WRN
related resource Werner Syndrome mutation database
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
tumoral somatic mutation      
missense mutations or polymorphisms could promote genetic instability and cancer by selectively interfering with recombination in somatic cells
tumoral     --low  
deficiency is associated with accumulation of gaps and breaks at common fragile sites even under unperturbed conditions
Susceptibility
  • to age related disorders such as atherosclerosis
  • to enhanced longevity
  • Variant & Polymorphism SNP L1074F, C1367R
    Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    cancerhead and neck 
    RECQL and WRN proteins are potential therapeutic targets in head and neck squamous cell carcinoma
    ANIMAL & CELL MODELS