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 -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 315
Individuals with public variants 0
Hidden variants -

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 HGNC:12791
Entrez Gene 7486
PubMed articles WRN
OMIM - Gene 604611


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     
00021063 8 Werner syndrome, RecQ helicase-like NM_000553.4 NP_000544.2