1. Gene
  2. Wrn - WRN RecQ like helicase Gene

Wrn - WRN RecQ like helicase Gene

Rattus norvegicus

Also known as RGD1564788

Gene ID: 290805 | Gene type: protein coding

About Wrn

Summary

Enables chromatin binding activity. Involved in brain development. Located in neuron projection. Human ortholog(s) of this gene implicated in Werner syndrome; breast cancer; coronary artery disease (multiple); diffuse scleroderma; and senile cataract. Orthologous to human WRN (WRN RecQ like helicase). [provided by Alliance of Genome Resources, Apr 2022]

Wrn Products(2)

mRNA Protein Name
XM_006253256.4 XP_006253318.1 Werner syndrome ATP-dependent helicase isoform X1
XM_039095090.1 XP_038951018.1 Werner syndrome ATP-dependent helicase isoform X2
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables chromatin binding IDA
IDA: Inferred from direct assay
19737542 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

Werner syndrome ATP-dependent helicase

similar to Werner syndrome helicase homolog

Werner syndrome RecQ like helicase

Werner syndrome, RecQ helicase-like

Orthologs Information

Species Symbol Source ID
Homo sapiens Wrn NCBI NCBI:7486