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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 |
|---|---|---|---|
| 31 | ACACA | acetyl-CoA carboxylase alpha | |
| 48 | ACO1 | aconitase 1 | |
| 250 | ALPP | alkaline phosphatase, placental | |
| 308 | ANXA5 | annexin A5 | |
| 410 | ARSA | arylsulfatase A | |
| 811 | CALR | calreticulin | |
| 847 | CAT | catalase | |
| 1594 | CYP27B1 | cytochrome P450 family 27 subfamily B member 1 | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O14561 | Acyl carrier protein, mitochondrial | |
| O15228 | Dihydroxyacetone phosphate acyltransferase | |
| P04040 | Catalase | |
| P04156 | Major prion protein | |
| P05187 | Alkaline phosphatase, placental type | |
| P07203 | Glutathione peroxidase 1 | |
| P08758 | Annexin A5 | |
| P11413 | Glucose-6-phosphate 1-dehydrogenase | |
| P12821 | Angiotensin-converting enzyme | |
| P14778 | Interleukin-1 receptor type 1 |
