Gene: Wrn (Werner syndrome, RecQ helicase-like) Rattus norvegicus
Symbol: Wrn
Name: Werner syndrome, RecQ helicase-like
Description: ENCODES a protein that exhibits chromatin binding; 3'-5' DNA helicase activity (ortholog); 3'-5' exonuclease activity (ortholog); INVOLVED IN brain development; base-excision repair (ortholog); cell aging (ortholog); ASSOCIATED WITH Breast Neoplasms (ortholog); Cardiomyopathy, Restrictive (ortholog); Coronary Artery Disease (ortholog); FOUND IN neuron projection; centrosome (ortholog); MutLalpha complex (ortholog); INTERACTS WITH cisplatin; ketamine; 2,3,7,8-tetrachlorodibenzodioxine (ortholog)
Type: protein-coding
RefSeq Status: MODEL
Also known as: LOC290805; RGD1564788; similar to Werner syndrome helicase homolog
Orthologs:
Latest Assembly: RGSC Genome Assembly v5.0
Position:
MapChrPositionStrandSource
RGSC Genome Assembly v6.01662,483,751 - 62,618,936+NCBI
Rat Cytogenetic Map16q12.3 NCBI
RGSC Genome Assembly v5.01662,148,560 - 62,283,748+NCBI
RGSC Genome Assembly v3.41662,535,144 - 62,668,700+NCBI
Rat Celera Assembly1656,796,905 - 56,929,877+NCBI
Model

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Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (RGSC Genome Assembly v5.0)

Sequence

Nucleotide Sequences
Protein Sequences

Strain Variation

Strain Sequence Variants

Additional Information

External Database Links
Nomenclature History
 
More on Wrn
Entrez Gene
Ensembl Gene
GBrowse
JBrowse
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1564788
Created: 2006-02-09
Species: Rattus norvegicus
Last Modified: 2015-06-09
Status: ACTIVE