The WRN gene homepage

General information
Gene symbol WRN
Gene name Werner syndrome, RecQ helicase-like
Chromosome 8
Chromosomal band p12
Imprinted Unknown
Genomic reference NG_008870.1
Transcript reference NM_000553.4
Associated with diseases WRN
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 102
Unique public DNA variants reported 79
Individuals with public variants 129
Hidden variants 14
Date created September 13, 2012
Date last updated September 15, 2020
Version WRN:200915

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 12791
Entrez Gene 7486
PubMed articles WRN
OMIM - Gene 604611
OMIM - Diseases WRN (syndrome, Werner (WRN))
GeneCards WRN
GeneTests WRN
Orphanet WRN

Active transcripts




NCBI ID     

NCBI Protein ID     

00001669 8 Werner syndrome, RecQ helicase-like NM_000553.4 NP_000544.2 102

Copyright & disclaimer
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