WRN Chromosome 8

WRN RecQ like helicase
455 variants 455 Health Risk

Upload your DNA to see your personal genotypes for variants in WRN.

What This Gene Does
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 Info
Gene Group
"Exonucleases|RecQ like helicases"
Locus Type
gene with protein product
Location
8p12
Ensembl
ENSG00000165392
Associated Conditions (19)
Werner syndrome
Inborn genetic diseases
WRN-related disorder
Wiskott-Aldrich syndrome
Ovarian cancer
Colon adenocarcinoma
Colorectal cancer
Gastric cancer
Ovarian serous cystadenocarcinoma
Chronic lymphocytic leukemia/small lymphocytic lymphoma
Cervical cancer
Clear cell carcinoma of kidney
Malignant tumor of esophagus
Familial cancer of breast
Hereditary cancer
Papillary renal cell carcinoma type 1
Progressive pulmonary failure
6 conditions
Medulloblastoma
Key Variants
All Variants (455)
RSID Category Clinical Significance Conditions
RS779012596 Health Risk Pathogenic Werner syndrome, Werner syndrome
RS878854133 Health Risk Pathogenic Werner syndrome, Werner syndrome, Werner syndrome
RS878854135 Health Risk Pathogenic Werner syndrome, Werner syndrome
RS878854136 Health Risk Pathogenic Werner syndrome, Werner syndrome
RS924770060 Health Risk Pathogenic Werner syndrome, Werner syndrome
RS985347750 Health Risk Pathogenic Werner syndrome, Werner syndrome
RS1198210848 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1279240593 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1284409960 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1319491415 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1377977559 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1563338855 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1563339062 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1563376347 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1563376793 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1563385391 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1585409238 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1585427471 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1585440064 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1585440764 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1585478303 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS17847577 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Medulloblastoma, Werner syndrome
RS1802222407 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1813280584 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1813285283 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1813759748 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS1814195192 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2130118911 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2130306367 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2130322576 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2130469632 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2130469991 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2535911235 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2535927271 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS2535934098 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS281865157 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS281865160 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS370324188 Health Risk Pathogenic/Likely pathogenic Werner syndrome, WRN-related disorder, Werner syndrome
RS371720457 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS377215256 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome, Werner syndrome
RS745905108 Health Risk Pathogenic/Likely pathogenic Werner syndrome, WRN-related disorder, Werner syndrome
RS747319628 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS747587698 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS748484883 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS757808169 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS758988621 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS761240520 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS762379051 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS766733097 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
RS774007667 Health Risk Pathogenic/Likely pathogenic Werner syndrome, Werner syndrome
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