Gene: Wrn (Werner syndrome, RecQ helicase-like) Rattus norvegicus
Symbol: Wrn
Name: Werner syndrome, RecQ helicase-like
Description: ENCODES a protein that exhibits 3'-5' DNA helicase activity (ortholog); 3'-5' exonuclease activity (ortholog); ATP-dependent DNA helicase activity (ortholog); INVOLVED IN ATP catabolic process (ortholog); base-excision repair (ortholog); cell aging (ortholog); ASSOCIATED WITH Cardiomyopathy, Restrictive (ortholog); Coronary Artery Disease (ortholog); Myocardial Infarction (ortholog); FOUND IN centrosome (ortholog); MutLalpha complex (ortholog); nucleolus (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 v3.4
Position:
MapChrPositionStrandSource
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 Assembly1656,796,902 - 56,928,501+NCBI
Model

Launch Genome Browser (GBrowse)


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

Genomics

Comparative Map Data
Position Markers

Sequence

Nucleotide Sequences
Protein Sequences

Strain Variation

Strain Sequence Variants

Additional Information

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

RGD Object Information
RGD ID: 1564788
Created: 2006-02-09
Species: Rattus norvegicus
Last Modified: 2014-06-26
Status: ACTIVE