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Parkinson's disease 23
Summary
- Synonym
-
- autosomal recessive early-onset Parkinson disease 23
- autosomal recessive early-onset Parkinson's disease 23
- Definition
- An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.
- Super Class
- autosomal recessive disease early-onset Parkinson's disease
External Links
- Disease Ontology
- DOID:0060896
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 9197 | SLC33A1 | solute carrier family 33 member 1 | |
| 9365 | KL | klotho | |
| 9536 | PTGES | prostaglandin E synthase | |
| 10159 | ATP6AP2 | ATPase H+ transporting accessory protein 2 | |
| 10327 | AKR1A1 | aldo-keto reductase family 1 member A1 | |
| 10457 | GPNMB | glycoprotein nmb | |
| 10724 | OGA | O-GlcNAcase | |
| 10728 | PTGES3 | prostaglandin E synthase 3 | |
| 10908 | PNPLA6 | patatin like phospholipase domain containing 6 | |
| 11332 | ACOT7 | acyl-CoA thioesterase 7 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 | |
| Q9Y2H2 | Phosphatidylinositide phosphatase SAC2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001257 | Spasticity |
| HP:0001332 | Dystonia |
| HP:0001337 | Tremor |
| HP:0001347 | Hyperreflexia |
| HP:0002014 | Diarrhea |
| HP:0002018 | Nausea |
| HP:0002019 | Constipation |
| HP:0002063 | Rigidity |
| HP:0002067 | Bradykinesia |
| HP:0002141 | Gait imbalance |
