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
Parkinson's disease 19A
Summary
- Synonym
-
- juvenile onset Parkinson disease 19A
- juvenile onset Parkinson's disease 19A
- Definition
- An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.
- Super Class
- autosomal recessive disease early-onset Parkinson's disease
External Links
- Disease Ontology
- DOID:0060891
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 64116 | SLC39A8 | solute carrier family 39 member 8 | |
| 64132 | XYLT2 | xylosyltransferase 2 | |
| 65078 | RTN4R | reticulon 4 receptor | |
| 79154 | DHRS11 | dehydrogenase/reductase 11 | |
| 79661 | NEIL1 | nei like DNA glycosylase 1 | |
| 79993 | ELOVL7 | ELOVL fatty acid elongase 7 | |
| 80270 | HSD3B7 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | |
| 80351 | TNKS2 | tankyrase 2 | |
| 132789 | GNPDA2 | glucosamine-6-phosphate deaminase 2 | |
| 151056 | PLB1 | phospholipase B1 |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0100543 | Cognitive impairment |
| HP:0100660 | Dyskinesia |
| HP:0100710 | Impulsivity |
| HP:0100785 | Insomnia |
