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Alzheimer's disease 1
Summary
- Synonym
-
- Alzheimer's disease 1, early onset
- Definition
- An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21.
- Super Class
- Alzheimer's disease autosomal dominant disease
External Links
- Disease Ontology
- DOID:0080348
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 6484 | ST3GAL4 | ST3 beta-galactoside alpha-2,3-sialyltransferase 4 | |
| 6489 | ST8SIA1 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | |
| 6515 | SLC2A3 | solute carrier family 2 member 3 | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 6610 | SMPD2 | sphingomyelin phosphodiesterase 2 | |
| 6646 | SOAT1 | sterol O-acyltransferase 1 | |
| 6713 | SQLE | squalene epoxidase | |
| 6900 | CNTN2 | contactin 2 | |
| 7086 | TKT | transketolase | |
| 7108 | TM7SF2 | transmembrane 7 superfamily member 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q99685 | Monoglyceride lipase | |
| Q99798 | Aconitate hydratase, mitochondrial | |
| Q9BV94 | ER degradation-enhancing alpha-mannosidase-like protein 2 | |
| Q9BVK6 | Transmembrane emp24 domain-containing protein 9 | |
| Q9BXN2 | C-type lectin domain family 7 member A | |
| Q9BZR6 | Reticulon-4 receptor | |
| Q9H4A9 | Dipeptidase 2 | |
| Q9H7Z7 | Prostaglandin E synthase 2 | |
| Q9NNX6 | CD209 antigen | |
| Q9NPH3 | Interleukin-1 receptor accessory protein |
