Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Werner syndrome
Summary
- Synonym
-
- WS
- Werner's syndrome
- adult premature ageing syndrome
- adult progeria
- Definition
- A progeroid syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8.
- Super Class
- autosomal recessive disease progeroid syndrome
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 9365 | KL | klotho | |
| 22925 | PLA2R1 | phospholipase A2 receptor 1 | |
| 22933 | SIRT2 | sirtuin 2 | |
| 51548 | SIRT6 | sirtuin 6 | |
| 55556 | ENOSF1 | enolase superfamily member 1 | |
| 79661 | NEIL1 | nei like DNA glycosylase 1 | |
| 151056 | PLB1 | phospholipase B1 | |
| 159371 | SLC35G1 | solute carrier family 35 member G1 |
