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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Wilson disease
Summary
- Synonym
-
- Cerebral pseudosclerosis
- Westphal pseudosclerosis
- Westphal-Strumpell syndrome
- Wilson's disease
- hepatolenticular degeneration
- Definition
- A metal metabolism disease that is characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes.
- Super Class
- metal metabolism disorder
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2588 | GALNS | galactosamine (N-acetyl)-6-sulfatase | |
| 2752 | GLUL | glutamate-ammonia ligase | |
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3554 | IL1R1 | interleukin 1 receptor type 1 | |
| 4706 | NDUFAB1 | NADH:ubiquinone oxidoreductase subunit AB1 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 6609 | SMPD1 | sphingomyelin phosphodiesterase 1 | |
| 6718 | AKR1D1 | aldo-keto reductase family 1 member D1 | |
| 7412 | VCAM1 | vascular cell adhesion molecule 1 | |
| 8443 | GNPAT | glyceronephosphate O-acyltransferase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P15104 | Glutamine synthetase | |
| P15289 | Arylsulfatase A | |
| P17405 | Sphingomyelin phosphodiesterase | |
| P19320 | Vascular cell adhesion protein 1 | |
| P21399 | Cytoplasmic aconitate hydratase | |
| P27797 | Calreticulin | |
| P34059 | N-acetylgalactosamine-6-sulfatase | |
| Q13085 | Acetyl-CoA carboxylase 1 | |
| Q5VV63 | Attractin-like protein 1 | |
| Q6ZVN8 | Hemojuvelin |
