Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | WRN | contributors: mct/ - updated : 23-08-2019 |
HGNC name | Werner syndrome, RecQ helicase-like |
HGNC id | 12791 |
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ASSOCIATED DISORDERS |
corresponding disease(s) | WRN |
related resource | Werner Syndrome mutation database |
Susceptibility |
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Variant & Polymorphism SNP | L1074F, C1367R |
Candidate gene
Marker
| Therapy target
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ANIMAL & CELL MODELS |